Pathogenic variants in the human m6A reader YTHDC2 are associated with primary ovarian insufficiency

被引：0
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作者：
McGlacken-Byrne, Sinead M. [1 ,2 ]
Torres, Ignacio Del Valle [1 ]
Stabej, Polona Le Quesne [3 ,4 ]
Belutti, Laura [5 ]
Ocaka, Louise [3 ]
Ishida, Miho [1 ]
Suntharalingham, Jenifer P. [1 ]
Dattani, Mehul T. [1 ]
Kelberman, Dan [3 ]
Lagos, Carlos F. [8 ,9 ]
Livera, Gabriel [5 ]
Conway, Gerard S. [2 ]
Achermann, John C. [1 ]
机构：
[1] UCL, UCL Great Ormond St Inst Child Hlth, Genet & Genom Med, London, England
[2] UCL, Inst Womens Hlth, London, England
[3] UCL, UCL Great Ormond St Inst Child Hlth, GOSgene, Genet & Genom Med, London, England
[4] Univ Auckland, Dept Mol Med & Pathol, Auckland, New Zealand
[5] Univ Paris Saclay, Univ Paris, UMR Genet Stabil Stem Cells & Radiat E008, Lab Dev Gonads,CEA, Paris, France
[6] UCL, Zayed Ctr Res Rare Dis Children, London, England
[7] UCL, UCL Great Ormond St Inst Child Hlth, Dev Biol & Canc, London, England
[8] Pontificia Univ Catolica Chile, Dept Endocrinol, Santiago, Chile
[9] Univ San Sebastian, Santiago, Chile
来源：
HORMONE RESEARCH IN PAEDIATRICS | 2021年 / 94卷 / SUPPL 1期
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
P1-50
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收藏
页码：93 / 93
页数：1
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