Genetic founder effect at the hereditary neuralgic amyotrophy (HNA) locus on chromosome 17q25.

被引:0
|
作者
Watts, GDJ [1 ]
O'Briant, KC [1 ]
Chance, PF [1 ]
机构
[1] Univ Washington, Seattle, WA 98195 USA
关键词
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
2027
引用
收藏
页码:527 / 527
页数:1
相关论文
共 44 条
  • [21] Investigation of the chromosome 17q25 PSORS2 locus in atopic dermatitis
    Morar, N
    Bowcock, AM
    Harper, J
    Cookson, WO
    Moffatt, MF
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2005, 125 (03) : A25 - A25
  • [22] Investigation of the chromosome 17q25 PSORS2 locus in atopic dermatitis
    Morar, Nilesh
    Bowcock, Anne M.
    Harper, John I.
    Cookson, William O. C. M.
    Moffatt, Miriam F.
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2006, 126 (03) : 603 - 606
  • [23] Refinement of a psoriasis locus at chromosome 17q24-q25 (PSORS2) with association mapping.
    Bowcock, AM
    Helms, C
    Speckman, RA
    Menter, A
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 349 - 349
  • [24] Association Between Genetic Variants on Chromosome 15q25 Locus and Objective Measures of Tobacco Exposure
    Munafo, Marcus R.
    Timofeeva, Maria N.
    Morris, Richard W.
    Prieto-Merino, David
    Sattar, Naveed
    Brennan, Paul
    Johnstone, Elaine C.
    Relton, Caroline
    Johnson, Paul C. D.
    Walther, Donna
    Whincup, Peter H.
    Casas, Juan P.
    Uhl, George R.
    Vineis, Paolo
    Padmanabhan, Sandosh
    Jefferis, Barbara J.
    Amuzu, Antoinette
    Riboli, Elio
    Upton, Mark N.
    Aveyard, Paul
    Ebrahim, Shah
    Hingorani, Aroon D.
    Watt, Graham
    Palmer, Tom M.
    Timpson, Nicholas J.
    Smith, George Davey
    JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2012, 104 (10): : 740 - 748
  • [25] Hereditary frontotemporal dementia is linked to chromosome 17q21-q22: A genetic and clinicopathological study of three Dutch families
    Heutink, P
    Stevens, M
    Rizzu, P
    Bakker, E
    Kros, JM
    Tibben, A
    Niermeijer, MF
    vanDuijn, CM
    Oostra, BA
    vanSwieten, JC
    ANNALS OF NEUROLOGY, 1997, 41 (02) : 150 - 159
  • [26] Haplotype analysis of sporadic-idiopathic and hereditary brachial plexus neuropathy patients at 17q25 supports a founder mutation and genetic susceptibility among rare sporadic cases
    Klein, CJ
    Wu, YH
    Anderson, SA
    Klein, DM
    Atkinson, EJ
    Cunningham, JM
    Friedenberg, SM
    Dyck, JP
    Dyck, PJ
    NEUROLOGY, 2005, 64 (06) : A57 - A57
  • [27] Genetic Variation and Recurrent Haplotypes on Chromosome 6q23-25 Risk Locus in Familial Lung Cancer
    Musolf, Anthony M.
    Simpson, Claire L.
    Moiz, Bilal A.
    Pikielny, Claudio W.
    Middlebrooks, Candace D.
    Mandal, Diptasri
    de Andrade, Mariza
    Cole, Michael D.
    Gaba, Colette
    Yang, Ping
    You, Ming
    Li, Yafang
    Kupert, Elena Y.
    Anderson, Marshall W.
    Schwartz, Ann G.
    Pinney, Susan M.
    Amos, Christopher, I
    Bailey-Wilson, Joan E.
    CANCER RESEARCH, 2021, 81 (12) : 3162 - 3173
  • [28] HOLISTIC VISUALIZATION OF THE ACID α-GLUCOSIDASE LOCUS ON CHROMOSOME 17Q25 AND ITS MUTATIONS WITHIN THE COMPLEXITY OF THE GENOME ORGANIZATION
    Kroos, M.
    Lesnussa, M.
    de Klein, A.
    van der Ploeg, A.
    Reuser, A.
    Knoch, T.
    Eussen, B.
    CLINICAL THERAPEUTICS, 2010, 32 : S78 - S78
  • [29] Cia27 is a novel non-MHC arthritis severity locus on rat chromosome 10 syntenic to the rheumatoid arthritis 17q22-q25 locus
    Brenner, M.
    Laragione, T.
    Yarlett, N. C.
    Li, W.
    Mello, A.
    Gulko, P. S.
    GENES AND IMMUNITY, 2006, 7 (05) : 335 - 341
  • [30] A new locus for late-onset, progressive, hereditary hearing loss DFNA20 maps to 17q25
    Morell, RJ
    Friderici, KH
    Wei, SN
    Elfenbein, JL
    Friedman, TB
    Fisher, RA
    GENOMICS, 2000, 63 (01) : 1 - 6