Novel mutations in CRB1 and ABCA4 genes cause Leber...

European Journal of Human Genetics 2013 / 11 Vol. 21; Iss. 11

Novel mutations in CRB1 and ABCA4 genes cause Leber congenital amaurosis and Stargardt disease in a Swedish family

Jonsson, Frida, Burstedt, Marie S, Sandgren, Ola, Norberg, Anna, Golovleva, Irina
How much do you like this book?
What’s the quality of the file?
Download the book for quality assessment
What’s the quality of the downloaded files?
Volume:
21
Language:
english
Journal:
European Journal of Human Genetics
DOI:
10.1038/ejhg.2013.23
Date:
November, 2013
File:
PDF, 788 KB
english, 2013
Conversion to is in progress
Conversion to is failed