A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants-Reference-Cited by-同舟云学术

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A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants

Published:2001-03-01 Issue:2 Volume:108 Page:91-97
ISSN:0340-6717
Container-title:Human Genetics
language:
Short-container-title:Human Genetics

Author:

Boycott Kym,Maybaum Tracy,Naylor Margaret,Weleber Richard,Robitaille Johane,Miyake Yozo,Bergen Arthur,Pierpont Mary,Pearce William,Bech-Hansen N.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s004390100461.pdf

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