A further observation of corneal dystrophy and perceptive deafness in two siblings-Reference-Cited by-同舟云学术

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A further observation of corneal dystrophy and perceptive deafness in two siblings

Published:1997-01 Issue:2 Volume:18 Page:87-91
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Magli A.,Capasso L.,Foà T.,Maurino V.,Ventruto V.

Publisher

Informa UK Limited

Subject

Genetics(clinical),Ophthalmology,Pediatrics, Perinatology, and Child Health

Link

http://www.tandfonline.com/doi/pdf/10.3109/13816819709057120

Reference9 articles.

1. Congenital Corneal Dystrophy

2. Buyse M L. Birth Defects Encyclopaedia. Blackwell, Cambridge 1990; 451–452, 1870

Cited by 9 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. The genetics of Fuchs’ corneal dystrophy;Expert Review of Ophthalmology;2012-08

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

3. Slc4a11 Gene Disruption in Mice;Journal of Biological Chemistry;2009-09

4. Congenital hereditary endothelial dystrophy with progressive sensorineural deafness (Harboyan syndrome);Orphanet Journal of Rare Diseases;2008-10-15

5. Autosomal Recessive CHED Associated With Novel Compound Heterozygous Mutations in SLC4A11;Cornea;2007-08

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