Characterization of a mutation within the NDP gene in a family with a manifesting female carrier-Reference-Cited by-同舟云学术

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Characterization of a mutation within the NDP gene in a family with a manifesting female carrier

Published:1993 Issue:10 Volume:2 Page:1727-1729
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum Mol Genet

Author:

Chen Z.-Y.,Battinelli E.M.,Woodruff G.,Young I.,Breakfield X.O.,Craig I.W.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/2/10/1727/1787498/2-10-1727.pdf

Cited by 31 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Characterization of a novel heterozygous frameshift variant in NDP gene that causes familial exudative vitreoretinopathy in female patients;Molecular Genetics and Genomics;2024-03-13

2. Whole-Exome Sequencing Reveals Novel NDP Variants in X-Linked Familial Exudative Vitreoretinopathy;European Journal of Ophthalmology;2022-01-17

3. Pediatric Retinal Vascular Diseases;Albert and Jakobiec's Principles and Practice of Ophthalmology;2022

4. Pediatric Retinal Vascular Diseases;Albert and Jakobiec's Principles and Practice of Ophthalmology;2021

5. Familial exudative vitreoretinopathy and related retinopathies;Eye;2014-10-17

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