Identification of gene mutations in pediatric cardiomyopathy by whole exome sequencing

被引:0
|
作者
Rojnueangnit, K. [1 ]
Sirichongkolthong, B. [1 ]
Wongwandee, R. [1 ]
Khetkham, T. [1 ]
Noojarern, S. [2 ]
Khongkraparn, A. [2 ]
Wattanasirichaigoon, D. [2 ]
机构
[1] Thammasat Univ, Klongluang, Thailand
[2] Mahidol Univ, Ramathibodi Hosp, Bangkok, Thailand
关键词
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
P05.11C
引用
收藏
页码:137 / 137
页数:1
相关论文
共 50 条
  • [1] Identification of Gene Mutations in Primary Pediatric Cardiomyopathy by Whole Exome Sequencing
    Rojnueangnit, Kitiwan
    Sirichongkolthong, Boonchu
    Wongwandee, Ratthapon
    Khetkham, Thanitchet
    Noojarern, Saisuda
    Khongkraparn, Arthaporn
    Wattanasirichaigoon, Duangrurdee
    PEDIATRIC CARDIOLOGY, 2020, 41 (01) : 165 - 174
  • [2] Identification of Gene Mutations in Primary Pediatric Cardiomyopathy by Whole Exome Sequencing
    Kitiwan Rojnueangnit
    Boonchu Sirichongkolthong
    Ratthapon Wongwandee
    Thanitchet Khetkham
    Saisuda Noojarern
    Arthaporn Khongkraparn
    Duangrurdee Wattanasirichaigoon
    Pediatric Cardiology, 2020, 41 : 165 - 174
  • [3] Whole Exome Sequencing Reveals Spectrum of Gene Mutations in Pediatric AML
    Shiba, Norio
    Yoshida, Kenichi
    Okuno, Yusuke
    Shiraishi, Yuichi
    Nagata, Yasunobu
    Ohki, Kentarou
    Kato, Motohiro
    Park, Myoung-ja
    Takita, Junko
    Kanazawa, Takashi
    Kudo, Kazuko
    Arakawa, Hirokazu
    Ito, Etsuro
    Sanada, Masashi
    Miyano, Satoru
    Ogawa, Seishi
    Hayashi, Yasuhide
    BLOOD, 2012, 120 (21)
  • [4] IDENTIFICATION OF TARGETABLE MUTATIONS IN RARE PEDIATRIC BRAIN TUMORS BY CLINICAL WHOLE EXOME SEQUENCING
    Lin, Frank Y.
    Bavle, Abhishek
    Wheeler, David
    Gibbs, Richard
    Lam, Sandi
    Su, Jack
    Chintagumpala, Murali
    Adesina, Adekunle
    Roy, Angshumoy
    Plon, Sharon E.
    Parsons, D. Williams
    NEURO-ONCOLOGY, 2015, 17 : 8 - 8
  • [5] NOVEL MUTATIONS IN FAMILIAL DILATED CARDIOMYOPATHY IDENTIFIED BY WHOLE EXOME SEQUENCING
    Tadros, R.
    Chami, N.
    Beaudoin, M.
    Lo, K.
    Robb, L.
    Lemarbre, F.
    Talajic, M.
    Lettre, G.
    CANADIAN JOURNAL OF CARDIOLOGY, 2013, 29 (10) : S364 - S364
  • [6] Identification of Novel TTN Mutations in Three Chinese Familial Dilated Cardiomyopathy Pedigrees by Whole Exome Sequencing
    Peng, Ying
    Miao, Jinxin
    Zhai, Yafei
    Fang, Guangming
    Wang, Chuchu
    Wang, Yaohe
    Zhao, Xiaoyan
    Dong, Jianzeng
    CARDIOVASCULAR INNOVATIONS AND APPLICATIONS, 2020, 4 (04) : 229 - 237
  • [7] IDENTIFICATION OF SOMATIC AND GERMLINE MUTATIONS USING WHOLE EXOME SEQUENCING OF HEPATOBLASTOMA
    Hoshino, N.
    Nishimura, R.
    Seki, M.
    Okuno, Y.
    Shiraishi, Y.
    Sato, Y.
    Yoshida, K.
    Miyano, S.
    Hahashi, Y.
    Iwanaka, T.
    Ogawa, S.
    Takita, J.
    PEDIATRIC BLOOD & CANCER, 2013, 60 : 18 - 18
  • [8] Rapid identification of kidney cyst mutations by whole exome sequencing in zebrafish
    Ryan, Sean
    Willer, Jason
    Marjoram, Lindsay
    Bagwell, Jennifer
    Mankiewicz, Jamie
    Leshchiner, Ignaty
    Goessling, Wolfram
    Bagnat, Michel
    Katsanis, Nicholas
    DEVELOPMENT, 2013, 140 (21): : 4445 - 4451
  • [9] Identification of mutations in retinal disease genes using Whole Exome Sequencing
    Mayer, Anja Kathrin
    Wissinger, Bernd
    Weisschuh, Nicole
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2015, 56 (07)
  • [10] Gene Identification in Axonopathies by Applying Massive Whole Exome Sequencing
    Zuchner, Stephan
    Gonzalez, Michael
    Schuele, Rebecca
    Siskind, Carly
    Powell, Eric
    Montenegro, Gladys
    Shengru, Guo
    Blanton, Susan
    Beecham, Gary
    Speziani, Fiorella
    Deconinck, Tine
    Young, Peter
    Kennerson, Marina
    Nicholson, Garth
    De Jonghe, Peter
    Vance, Jeffery
    Schoels, Ludger
    Menezes, Manoj
    Herrmann, David
    Scherer, Steven
    Reilly, Mary
    Shy, Mike
    Zuchner, Stephan
    NEUROLOGY, 2012, 78