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- [11] Preclinical Use of a New scAAV9/SUMF1 Vector for the Treatment of Multiple Sulfatase DeficiencyMOLECULAR THERAPY, 2022, 30 (04) : 476 - 476Presa, Maximiliano论文数: 0 引用数: 0 h-index: 0机构: Jackson Lab, 600 Main St, Bar Harbor, ME 04609 USA Jackson Lab, 600 Main St, Bar Harbor, ME 04609 USABailey, Rachel M.论文数: 0 引用数: 0 h-index: 0机构: Univ Texas Southwestern Med Ctr Dallas, Dallas, TX 75390 USA Jackson Lab, 600 Main St, Bar Harbor, ME 04609 USARay, Somdatta论文数: 0 引用数: 0 h-index: 0机构: Jackson Lab, 600 Main St, Bar Harbor, ME 04609 USA Jackson Lab, 600 Main St, Bar Harbor, ME 04609 USABailey, Lauren论文数: 0 引用数: 0 h-index: 0机构: Univ Texas Southwestern Med Ctr Dallas, Dallas, TX 75390 USA Jackson Lab, 600 Main St, Bar Harbor, ME 04609 USATata, Saurabh论文数: 0 引用数: 0 h-index: 0机构: Jackson Lab, 600 Main St, Bar Harbor, ME 04609 USA Jackson Lab, 600 Main St, Bar Harbor, ME 04609 USAMurphy, Tara论文数: 0 引用数: 0 h-index: 0机构: Jackson Lab, 600 Main St, Bar Harbor, ME 04609 USA Jackson Lab, 600 Main St, Bar Harbor, ME 04609 USACoombs, Harold论文数: 0 引用数: 0 h-index: 0机构: Jackson Lab, 600 Main St, Bar Harbor, ME 04609 USA Jackson Lab, 600 Main St, Bar Harbor, ME 04609 USAGray, Steven J.论文数: 0 引用数: 0 h-index: 0机构: Univ Texas Southwestern Med Ctr Dallas, Dallas, TX 75390 USA Jackson Lab, 600 Main St, Bar Harbor, ME 04609 USALutz, Cathleen论文数: 0 引用数: 0 h-index: 0机构: Jackson Lab, 600 Main St, Bar Harbor, ME 04609 USA Jackson Lab, 600 Main St, Bar Harbor, ME 04609 USA
- [12] Late infantile form of multiple sulfatase deficiency with a novel missense variant in the SUMF1 gene: case report and reviewBMC PEDIATRICS, 2023, 23 (01)Sheth, Jayesh论文数: 0 引用数: 0 h-index: 0机构: FRIGEs Inst Human Genet, FRIGE House,Jodhpur Gam Rd, Ahmadabad, India FRIGEs Inst Human Genet, FRIGE House,Jodhpur Gam Rd, Ahmadabad, IndiaShah, Siddharth论文数: 0 引用数: 0 h-index: 0机构: Royal Inst Child Neurosci, Ahmadabad, India FRIGEs Inst Human Genet, FRIGE House,Jodhpur Gam Rd, Ahmadabad, IndiaDatar, Chaitanya论文数: 0 引用数: 0 h-index: 0机构: Bharati Hosp & Res Ctr, Pune, India KEM Hosp, Pune, India FRIGEs Inst Human Genet, FRIGE House,Jodhpur Gam Rd, Ahmadabad, IndiaBhatt, Kaveri论文数: 0 引用数: 0 h-index: 0机构: FRIGEs Inst Human Genet, FRIGE House,Jodhpur Gam Rd, Ahmadabad, India FRIGEs Inst Human Genet, FRIGE House,Jodhpur Gam Rd, Ahmadabad, IndiaRaval, Pooja论文数: 0 引用数: 0 h-index: 0机构: FRIGEs Inst Human Genet, FRIGE House,Jodhpur Gam Rd, Ahmadabad, India FRIGEs Inst Human Genet, FRIGE House,Jodhpur Gam Rd, Ahmadabad, IndiaNair, Aadhira论文数: 0 引用数: 0 h-index: 0机构: FRIGEs Inst Human Genet, FRIGE House,Jodhpur Gam Rd, Ahmadabad, India FRIGEs Inst Human Genet, FRIGE House,Jodhpur Gam Rd, Ahmadabad, IndiaJain, Deepika论文数: 0 引用数: 0 h-index: 0机构: Shishu Child Dev & Early Intervent Ctr, Ahmadabad, India FRIGEs Inst Human Genet, FRIGE House,Jodhpur Gam Rd, Ahmadabad, IndiaShah, Jhanvi论文数: 0 引用数: 0 h-index: 0机构: FRIGEs Inst Human Genet, FRIGE House,Jodhpur Gam Rd, Ahmadabad, India FRIGEs Inst Human Genet, FRIGE House,Jodhpur Gam Rd, Ahmadabad, IndiaSheth, Frenny论文数: 0 引用数: 0 h-index: 0机构: FRIGEs Inst Human Genet, FRIGE House,Jodhpur Gam Rd, Ahmadabad, India FRIGEs Inst Human Genet, FRIGE House,Jodhpur Gam Rd, Ahmadabad, IndiaSheth, Harsh论文数: 0 引用数: 0 h-index: 0机构: FRIGEs Inst Human Genet, FRIGE House,Jodhpur Gam Rd, Ahmadabad, India FRIGEs Inst Human Genet, FRIGE House,Jodhpur Gam Rd, Ahmadabad, India
- [13] Natural Disease History and Characterization of SUMF1 Molecular Defects in Multiple Sulfatase Deficiency: a Case ReportINTERNATIONAL JOURNAL OF PEDIATRICS-MASHHAD, 2021, 9 (12): : 15047 - 15053Khanzadeh, Shokoufeh论文数: 0 引用数: 0 h-index: 0机构: Tabriz Univ Med Sci, Tabriz, Iran Tabriz Univ Med Sci, Tabriz, IranBabaei, Meisam论文数: 0 引用数: 0 h-index: 0机构: North Khorasan Univ Med Sci, Dept Pediat, Pediat Neurol, Bojnurd, Iran Tabriz Univ Med Sci, Tabriz, IranImanpour, Parvin论文数: 0 引用数: 0 h-index: 0机构: Tabriz Univ Med Sci, Children Hosp, Clin Res Dev Unit, Tabriz, Iran Tabriz Univ Med Sci, Tabriz, Iran论文数: 引用数: h-index:机构:
- [14] Preclinical studies to support the intrathecal delivery of scAAV9/SUMF1 as a gene replacement therapy for multiple sulfatase deficiencyMOLECULAR GENETICS AND METABOLISM, 2021, 132 (02) : S17 - S18Bailey, Rachel M.论文数: 0 引用数: 0 h-index: 0机构: Univ Texas Southwestern Med Ctr Dallas, Dallas, TX 75390 USA Univ Texas Southwestern Med Ctr Dallas, Dallas, TX 75390 USAPresa, Maximiliano论文数: 0 引用数: 0 h-index: 0机构: Jackson Lab, 600 Main St, Bar Harbor, ME 04609 USA Univ Texas Southwestern Med Ctr Dallas, Dallas, TX 75390 USARay, Somdatta论文数: 0 引用数: 0 h-index: 0机构: Jackson Lab, 600 Main St, Bar Harbor, ME 04609 USA Univ Texas Southwestern Med Ctr Dallas, Dallas, TX 75390 USABailey, Lauren论文数: 0 引用数: 0 h-index: 0机构: Univ Texas Southwestern Med Ctr Dallas, Dallas, TX 75390 USA Univ Texas Southwestern Med Ctr Dallas, Dallas, TX 75390 USACoombs, Harold论文数: 0 引用数: 0 h-index: 0机构: Jackson Lab, 600 Main St, Bar Harbor, ME 04609 USA Univ Texas Southwestern Med Ctr Dallas, Dallas, TX 75390 USAWalls, Randy论文数: 0 引用数: 0 h-index: 0机构: Jackson Lab, 600 Main St, Bar Harbor, ME 04609 USA Univ Texas Southwestern Med Ctr Dallas, Dallas, TX 75390 USALutz, Cathleen论文数: 0 引用数: 0 h-index: 0机构: Jackson Lab, 600 Main St, Bar Harbor, ME 04609 USA Univ Texas Southwestern Med Ctr Dallas, Dallas, TX 75390 USAGray, Steven J.论文数: 0 引用数: 0 h-index: 0机构: Univ Texas Southwestern Med Ctr Dallas, Dallas, TX 75390 USA Univ Texas Southwestern Med Ctr Dallas, Dallas, TX 75390 USA
- [15] Preclinical Gene Replacement Therapy with a New scAAV9/SUMF1 Viral Vector for the Treatment of Multiple Sulfatase DeficiencyMOLECULAR THERAPY, 2020, 28 (04) : 413 - 413Presa, Maximiliano论文数: 0 引用数: 0 h-index: 0机构: Jackson Lab, Rare & Orphan Dis Ctr, 600 Main St, Bar Harbor, ME 04609 USA Jackson Lab, Rare & Orphan Dis Ctr, 600 Main St, Bar Harbor, ME 04609 USABailey, Rachel M.论文数: 0 引用数: 0 h-index: 0机构: Univ Texas Southwestern Med Ctr Dallas, Dallas, TX 75390 USA Jackson Lab, Rare & Orphan Dis Ctr, 600 Main St, Bar Harbor, ME 04609 USARay, Somdatta论文数: 0 引用数: 0 h-index: 0机构: Jackson Lab, Rare & Orphan Dis Ctr, 600 Main St, Bar Harbor, ME 04609 USA Jackson Lab, Rare & Orphan Dis Ctr, 600 Main St, Bar Harbor, ME 04609 USACoombs, Harold论文数: 0 引用数: 0 h-index: 0机构: Jackson Lab, Rare & Orphan Dis Ctr, 600 Main St, Bar Harbor, ME 04609 USA Jackson Lab, Rare & Orphan Dis Ctr, 600 Main St, Bar Harbor, ME 04609 USAWalls, Randy论文数: 0 引用数: 0 h-index: 0机构: Jackson Lab, Rare & Orphan Dis Ctr, 600 Main St, Bar Harbor, ME 04609 USA Jackson Lab, Rare & Orphan Dis Ctr, 600 Main St, Bar Harbor, ME 04609 USAGray, Steven论文数: 0 引用数: 0 h-index: 0机构: Univ Texas Southwestern Med Ctr Dallas, Dallas, TX 75390 USA Jackson Lab, Rare & Orphan Dis Ctr, 600 Main St, Bar Harbor, ME 04609 USALutz, Cathleen论文数: 0 引用数: 0 h-index: 0机构: Jackson Lab, Rare & Orphan Dis Ctr, 600 Main St, Bar Harbor, ME 04609 USA Jackson Lab, Rare & Orphan Dis Ctr, 600 Main St, Bar Harbor, ME 04609 USA
- [16] Natural disease history and characterisation of SUMF1 molecular defects in ten unrelated patients with multiple sulfatase deficiencyORPHANET JOURNAL OF RARE DISEASES, 2015, 10论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Le Trionnaire, Emmanuelle论文数: 0 引用数: 0 h-index: 0机构: CHU Purpan, IFB, Lab Biochim Metab, Toulouse, France CHU Purpan, IFB, Lab Biochim Metab, Toulouse, FranceBednarek, Nathalie论文数: 0 引用数: 0 h-index: 0机构: CHU Reims, Serv Neonatol, Reims, France CHU Purpan, IFB, Lab Biochim Metab, Toulouse, FranceCaillaud, Catherine论文数: 0 引用数: 0 h-index: 0机构: Hop Necker Enfants Malad, Lab Biochim Metabol & Proteom, Paris, France CHU Purpan, IFB, Lab Biochim Metab, Toulouse, FranceChaix, Yves论文数: 0 引用数: 0 h-index: 0机构: Hop Enfants, CHU Purpan, Toulouse, France Univ Toulouse 3, CHU Purpan, INSERM, UMR Imagerie Cerebrale & Handicaps Neurol 825, F-31062 Toulouse, France CHU Purpan, IFB, Lab Biochim Metab, Toulouse, FranceDelrue, Marie-Ange论文数: 0 引用数: 0 h-index: 0机构: CHU Pellegrin, Serv Genet Med, Bordeaux, France Univ Bordeaux 2, Lab Malad Rares Genet & Metab, F-33076 Bordeaux, France CHU Purpan, IFB, Lab Biochim Metab, Toulouse, FranceDusser, Anne论文数: 0 引用数: 0 h-index: 0机构: CHU Bicetre, Serv Neuropediat, Le Kremlin Bicetre, France CHU Purpan, IFB, Lab Biochim Metab, Toulouse, FranceFroissart, Roseline论文数: 0 引用数: 0 h-index: 0机构: Hosp Civils Lyon, Ctr Biol & Pathol Est, Bron, France CHU Purpan, IFB, Lab Biochim Metab, Toulouse, FranceGarnotel, Roselyne论文数: 0 引用数: 0 h-index: 0机构: CHU Reims, Amer Mem Hosp, Lab Biol & Rech Pediat, Reims, France CHU Purpan, IFB, Lab Biochim Metab, Toulouse, FranceGuffon, Nathalie论文数: 0 引用数: 0 h-index: 0机构: Ctr Reference Malad Hereditaires Metab, Lyon, France CHU Purpan, IFB, Lab Biochim Metab, Toulouse, FranceMegarbane, Andre论文数: 0 引用数: 0 h-index: 0机构: Univ St Joseph, Unite Genet Med, Beirut, Lebanon Univ St Joseph, Lab Associe, INSERM, UMR S910, Beirut, Lebanon Inst Jerome Lejeune, Paris, France CHU Purpan, IFB, Lab Biochim Metab, Toulouse, Francede Baulny, Helene Ogier论文数: 0 引用数: 0 h-index: 0机构: CHU Robert Debre, AP HP, Ctr Reference Malad Hereditaires Metab, Paris, France CHU Purpan, IFB, Lab Biochim Metab, Toulouse, FrancePedespan, Jean-Michel论文数: 0 引用数: 0 h-index: 0机构: CHU Robert Debre, AP HP, Ctr Reference Malad Hereditaires Metab, Paris, France CHU Purpan, IFB, Lab Biochim Metab, Toulouse, FrancePichard, Samia论文数: 0 引用数: 0 h-index: 0机构: CHU Robert Debre, AP HP, Ctr Reference Malad Hereditaires Metab, Paris, France CHU Purpan, IFB, Lab Biochim Metab, Toulouse, FranceValayannopoulos, Vassili论文数: 0 引用数: 0 h-index: 0机构: Hop Necker Enfants Malad, Ctr Reference Malad Metab, Paris, France CHU Purpan, IFB, Lab Biochim Metab, Toulouse, FranceVerloes, Alain论文数: 0 引用数: 0 h-index: 0机构: CHU Robert Debre, Serv Genet Clin, Paris, France CHU Purpan, IFB, Lab Biochim Metab, Toulouse, FranceLevade, Thierry论文数: 0 引用数: 0 h-index: 0机构: CHU Purpan, IFB, Lab Biochim Metab, Toulouse, France Univ Toulouse 3, INSERM, CRCT, UMR 1037, F-31062 Toulouse, France CHU Purpan, IFB, Lab Biochim Metab, Toulouse, France
- [17] Natural disease history and characterisation of SUMF1 molecular defects in ten unrelated patients with multiple sulfatase deficiencyOrphanet Journal of Rare Diseases, 10Frédérique Sabourdy论文数: 0 引用数: 0 h-index: 0机构: CHU Purpan,Laboratoire de Biochimie Métabolique, IFBLionel Mourey论文数: 0 引用数: 0 h-index: 0机构: CHU Purpan,Laboratoire de Biochimie Métabolique, IFBEmmanuelle Le Trionnaire论文数: 0 引用数: 0 h-index: 0机构: CHU Purpan,Laboratoire de Biochimie Métabolique, IFBNathalie Bednarek论文数: 0 引用数: 0 h-index: 0机构: CHU Purpan,Laboratoire de Biochimie Métabolique, IFBCatherine Caillaud论文数: 0 引用数: 0 h-index: 0机构: CHU Purpan,Laboratoire de Biochimie Métabolique, IFBYves Chaix论文数: 0 引用数: 0 h-index: 0机构: CHU Purpan,Laboratoire de Biochimie Métabolique, IFBMarie-Ange Delrue论文数: 0 引用数: 0 h-index: 0机构: CHU Purpan,Laboratoire de Biochimie Métabolique, IFBAnne Dusser论文数: 0 引用数: 0 h-index: 0机构: CHU Purpan,Laboratoire de Biochimie Métabolique, IFBRoseline Froissart论文数: 0 引用数: 0 h-index: 0机构: CHU Purpan,Laboratoire de Biochimie Métabolique, IFBRoselyne Garnotel论文数: 0 引用数: 0 h-index: 0机构: CHU Purpan,Laboratoire de Biochimie Métabolique, IFBNathalie Guffon论文数: 0 引用数: 0 h-index: 0机构: CHU Purpan,Laboratoire de Biochimie Métabolique, IFBAndré Megarbane论文数: 0 引用数: 0 h-index: 0机构: CHU Purpan,Laboratoire de Biochimie Métabolique, IFBHélène Ogier de Baulny论文数: 0 引用数: 0 h-index: 0机构: CHU Purpan,Laboratoire de Biochimie Métabolique, IFBJean-Michel Pédespan论文数: 0 引用数: 0 h-index: 0机构: CHU Purpan,Laboratoire de Biochimie Métabolique, IFBSamia Pichard论文数: 0 引用数: 0 h-index: 0机构: CHU Purpan,Laboratoire de Biochimie Métabolique, IFBVassili Valayannopoulos论文数: 0 引用数: 0 h-index: 0机构: CHU Purpan,Laboratoire de Biochimie Métabolique, IFBAlain Verloes论文数: 0 引用数: 0 h-index: 0机构: CHU Purpan,Laboratoire de Biochimie Métabolique, IFBThierry Levade论文数: 0 引用数: 0 h-index: 0机构: CHU Purpan,Laboratoire de Biochimie Métabolique, IFB
- [18] SUMF1 mutations affecting stability and activity of formylglycine generating enzyme predict clinical outcome in multiple sulfatase deficiencyEuropean Journal of Human Genetics, 2011, 19 : 253 - 261Lars Schlotawa论文数: 0 引用数: 0 h-index: 0机构: Georg August University Göttingen,Department of Pediatrics and Pediatric NeurologyEva Charlotte Ennemann论文数: 0 引用数: 0 h-index: 0机构: Georg August University Göttingen,Department of Pediatrics and Pediatric NeurologyKarthikeyan Radhakrishnan论文数: 0 引用数: 0 h-index: 0机构: Georg August University Göttingen,Department of Pediatrics and Pediatric NeurologyBernhard Schmidt论文数: 0 引用数: 0 h-index: 0机构: Georg August University Göttingen,Department of Pediatrics and Pediatric NeurologyAnupam Chakrapani论文数: 0 引用数: 0 h-index: 0机构: Georg August University Göttingen,Department of Pediatrics and Pediatric NeurologyHans-Jürgen Christen论文数: 0 引用数: 0 h-index: 0机构: Georg August University Göttingen,Department of Pediatrics and Pediatric NeurologyHugo Moser论文数: 0 引用数: 0 h-index: 0机构: Georg August University Göttingen,Department of Pediatrics and Pediatric NeurologyBeat Steinmann论文数: 0 引用数: 0 h-index: 0机构: Georg August University Göttingen,Department of Pediatrics and Pediatric NeurologyThomas Dierks论文数: 0 引用数: 0 h-index: 0机构: Georg August University Göttingen,Department of Pediatrics and Pediatric NeurologyJutta Gärtner论文数: 0 引用数: 0 h-index: 0机构: Georg August University Göttingen,Department of Pediatrics and Pediatric Neurology
- [19] Preclinical use of a clinically-relevant scAAV9/SUMF1 vector for the treatment of multiple sulfatase deficiencyCOMMUNICATIONS MEDICINE, 2025, 5 (01):Presa, Maximiliano论文数: 0 引用数: 0 h-index: 0机构: Jackson Lab, Rare Dis Translat Ctr, Bar Harbor, ME 04609 USA Jackson Lab, Rare Dis Translat Ctr, Bar Harbor, ME 04609 USABailey, Rachel M.论文数: 0 引用数: 0 h-index: 0机构: Univ Texas Southwestern Med Ctr, Ctr Alzheimers & Neurodegenerat Dis, Dallas, TX USA Univ Texas SouthWestern Med Ctr, Dept Pediat, Dallas, TX 75390 USA Jackson Lab, Rare Dis Translat Ctr, Bar Harbor, ME 04609 USARay, Somdatta论文数: 0 引用数: 0 h-index: 0机构: Jackson Lab, Rare Dis Translat Ctr, Bar Harbor, ME 04609 USA Jackson Lab, Rare Dis Translat Ctr, Bar Harbor, ME 04609 USABailey, Lauren论文数: 0 引用数: 0 h-index: 0机构: Univ Texas Southwestern Med Ctr, Ctr Alzheimers & Neurodegenerat Dis, Dallas, TX USA Jackson Lab, Rare Dis Translat Ctr, Bar Harbor, ME 04609 USATata, Saurabh论文数: 0 引用数: 0 h-index: 0机构: Jackson Lab, Rare Dis Translat Ctr, Bar Harbor, ME 04609 USA Jackson Lab, Rare Dis Translat Ctr, Bar Harbor, ME 04609 USAMurphy, Tara论文数: 0 引用数: 0 h-index: 0机构: Jackson Lab, Rare Dis Translat Ctr, Bar Harbor, ME 04609 USA Jackson Lab, Rare Dis Translat Ctr, Bar Harbor, ME 04609 USAPiec, Pierre-Alexandre论文数: 0 引用数: 0 h-index: 0机构: Jackson Lab, Rare Dis Translat Ctr, Bar Harbor, ME 04609 USA Jackson Lab, Rare Dis Translat Ctr, Bar Harbor, ME 04609 USACombs, Harold论文数: 0 引用数: 0 h-index: 0机构: Jackson Lab, Rare Dis Translat Ctr, Bar Harbor, ME 04609 USA Jackson Lab, Rare Dis Translat Ctr, Bar Harbor, ME 04609 USAGray, Steven J.论文数: 0 引用数: 0 h-index: 0机构: Univ Texas SouthWestern Med Ctr, Dept Pediat, Dallas, TX 75390 USA Jackson Lab, Rare Dis Translat Ctr, Bar Harbor, ME 04609 USALutz, Cathleen论文数: 0 引用数: 0 h-index: 0机构: Jackson Lab, Rare Dis Translat Ctr, Bar Harbor, ME 04609 USA Jackson Lab, Rare Dis Translat Ctr, Bar Harbor, ME 04609 USA
- [20] A homozygous missense variant of SUMF1 in the Bedouin population extends the clinical spectrum in ultrarare neonatal multiple sulfatase deficiencyMOLECULAR GENETICS & GENOMIC MEDICINE, 2020, 8 (09):Staretz-Chacham, Orna论文数: 0 引用数: 0 h-index: 0机构: Ben Gurion Univ Negev, Soroka Univ Med Ctr, Metab Clin, Beer Sheva, Israel Ben Gurion Univ Negev, Soroka Univ Med Ctr, Neonatl Unit, Beer Sheva, Israel Ben Gurion Univ Negev, Soroka Univ Med Ctr, Div Pediat, Beer Sheva, Israel Ben Gurion Univ Negev, Soroka Univ Med Ctr, Metab Clin, Beer Sheva, IsraelSchlotawa, Lars论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr, Dept Paediat & Adolescent Med, Gottingen, Germany Ben Gurion Univ Negev, Soroka Univ Med Ctr, Metab Clin, Beer Sheva, IsraelWormser, Ohad论文数: 0 引用数: 0 h-index: 0机构: Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol Negev, Beer Sheva, Israel Ben Gurion Univ Negev, Fac Hlth Sci, Beer Sheva, Israel Ben Gurion Univ Negev, Shraga Segal Dept Microbiol Immunol & Genet, Beer Sheva, Israel Ben Gurion Univ Negev, Soroka Univ Med Ctr, Metab Clin, Beer Sheva, IsraelGolan-Tripto, Inbal论文数: 0 引用数: 0 h-index: 0机构: Ben Gurion Univ Negev, Soroka Univ Med Ctr, Div Pediat, Beer Sheva, Israel Ben Gurion Univ Negev, Soroka Univ Med Ctr, Metab Clin, Beer Sheva, IsraelBirk, Ohad S.论文数: 0 引用数: 0 h-index: 0机构: Ben Gurion Univ Negev, Morris Kahn Lab Human Genet, Natl Inst Biotechnol Negev, Beer Sheva, Israel Ben Gurion Univ Negev, Fac Hlth Sci, Beer Sheva, Israel Ben Gurion Univ Negev, Shraga Segal Dept Microbiol Immunol & Genet, Beer Sheva, Israel Ben Gurion Univ Negev, Soroka Univ Med Ctr, Genet Inst, Beer Sheva, Israel Ben Gurion Univ Negev, Soroka Univ Med Ctr, Metab Clin, Beer Sheva, IsraelFerreira, Carlos R.论文数: 0 引用数: 0 h-index: 0机构: NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USA Ben Gurion Univ Negev, Soroka Univ Med Ctr, Metab Clin, Beer Sheva, IsraelDierks, Thomas论文数: 0 引用数: 0 h-index: 0机构: Bielefeld Univ, Fac Chem, Biochem 1, Bielefeld, Germany Ben Gurion Univ Negev, Soroka Univ Med Ctr, Metab Clin, Beer Sheva, Israel论文数: 引用数: h-index:机构: