Whole exome sequencing identified a rare WT1 loss‐of‐function variant in a non‐syndromic POI patient-Reference-Cited by-同舟云学术

Whole exome sequencing identified a rare WT1 loss‐of‐function variant in a non‐syndromic POI patient

Published:2021-11-29 Issue:1 Volume:10 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Molec Gen & Gen Med

Author:

Wang Yingchen¹,Chen Qing¹²,Zhang Feng¹²³,Yang Xi¹²,Shang Lingyue¹,Ren Shuting¹,Pan Yuncheng¹,Zhou Zixue¹²,Li Guoqing¹,Fang Yunzheng¹²,Jin Li¹,Wu Yanhua¹³⁴^ORCID,Zhang Xiaojin¹³

Affiliation:

1. Obstetrics and Gynecology Hospital NHC Key Laboratory of Reproduction Regulation (Shanghai Institute of Planned Parenthood Research) School of Life Sciences Fudan University Shanghai China

2. Institute of Metabolism and Integrative Biology Fudan University Shanghai China

3. Shanghai Key Laboratory of Female Reproductive Endocrine Related Diseases Shanghai China

4. National Demonstration Center for Experimental Biology Education School of Life Sciences Fudan University Shanghai China

Funder

National Natural Science Foundation of China

National Key Research and Development Program of China

Natural Science Foundation of Shanghai

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

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