Novel mutation at the initiation codon in the Norrie disease gene in two Japanese families-Reference-Cited by-同舟云学术

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Novel mutation at the initiation codon in the Norrie disease gene in two Japanese families

Published:1995-01 Issue:1 Volume:95 Page:
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Isashiki Yasushi,Ohba Norio,Yanagita Toyoko,Hokita Naoko,Doi Norihito,Nakagawa Masanori,Ozawa Masayuki,Kuroda Noriko

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00225085.pdf

Cited by 14 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. Sequence and structure comparison of ATP synthase F0 subunits 6 and 8 in notothenioid fish;PLOS ONE;2021-10-06

2. Introgression of regulatory alleles and a missense coding mutation drive plumage pattern diversity in the rock pigeon;eLife;2018-07-17

3. A novel c.240_241insGG mutation in NDP gene in a family with Norrie disease;Clinical and Experimental Optometry;2018-03-01

4. A novel c.2T>ANDPmissense mutation in a Chinese family with Norrie disease;Acta Ophthalmologica;2015-11-07

5. Familial cases of Norrie disease detected by copy number analysis;Japanese Journal of Ophthalmology;2014-07-15

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