A new pedigree with recessive CHED mapping to the CHED2 locus on 20p13-Reference-Cited by-同舟云学术

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A new pedigree with recessive CHED mapping to the CHED2 locus on 20p13

Published:2001-06-01 Issue:6 Volume:85 Page:754.5-754
ISSN:0007-1161
Container-title:British Journal of Ophthalmology
language:en
Short-container-title:Br J Ophthalmol

Author:

MOHAMED MOIN D,McKIBBIN MARTIN,JAFRI HUSSEIN,RAASHED YASMIN,WOODS C GEOFFREY,INGLEHEARN CHRIS F

Publisher

BMJ

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Cited by 4 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. Autosomal recessive congenital hereditary corneal dystrophy associated with a novel SLC4A11 mutation in two consanguineous Tunisian families;British Journal of Ophthalmology;2021-04-20

2. Homozygous SLC4A11 mutation in a large Irish CHED2 pedigree;Ophthalmic Genetics;2016-04-08

3. Absence of Phenotype-Genotype Correlation of Patients Expressing Mutations in the SLC4A11 Gene;Cornea;2010-03

4. Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2);Nature Genetics;2006-06-11

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