Prenatal diagnosis of Walker–Warburg syndrome due to compound mutations in the <i>B3GALNT2</i> gene-Reference-Cited by-同舟云学术

Prenatal diagnosis of Walker–Warburg syndrome due to compound mutations in the B3GALNT2 gene

Author:

Wang Peng¹,Jin Pengzhen¹^ORCID,Zhu Linyan¹,Chen Min¹²,Qian Yeqing¹²,Zeng Wenshan¹,Wang Miaomiao¹,Xu Yuqing¹,Xu Yanfei¹,Dong Minyue¹²

Affiliation:

1. Women's Hospital School of Medicine Zhejiang University Hangzhou China

2. Key Laboratory of Reproductive Genetics (Zhejiang University), Ministry of Education Hangzhou China

Funder

National Natural Science Foundation of China

National Key Research and Development Program of China

Publisher

Wiley

Subject

Genetics (clinical),Drug Discovery,Genetics,Molecular Biology,Molecular Medicine

Link

Reference26 articles.

2. Klein C Congenital hydrocephalus in a Belgian draft horse associated with a nonsense mutation in B3GALNT2;Kolb DS;Can Vet J,2019

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