Comprehensive Genetic Analysis Unraveled the Missing Heritability in a Chinese Cohort With Wolfram Syndrome 1: Clinical and Genetic Findings-Reference-Cited by-同舟云学术

Comprehensive Genetic Analysis Unraveled the Missing Heritability in a Chinese Cohort With Wolfram Syndrome 1: Clinical and Genetic Findings

Published:2022-09-13 Issue:10 Volume:63 Page:9
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Zhang Xin¹,Xie Yue¹,Xu Ke¹,Chang Haoyu¹,Zhang Xiaohui¹,Li Yang¹

Affiliation:

1. Beijing Institute of Ophthalmology, Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University, Beijing Ophthalmology & Visual Sciences Key Lab. Beijing, China

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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4. Presentation and clinical course of Wolfram (DIDMOAD) syndrome from North India;Ganie;Diabet Med,2011

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