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

被引：0

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

引用

页码：93 / 93

页数：1

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