A novel, non-stop mutation in FOXE3 causes an autosomal...

European Journal of Human Genetics 2010 Vol. 19; Iss. 3

A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly

Doucette, Lance, Green, Jane, Fernandez, Bridget, Johnson, Gordon J, Parfrey, Patrick, Young, Terry-Lynn
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:
19
Year:
2010
Language:
english
Pages:
7
DOI:
10.1038/ejhg.2010.210
File:
PDF, 452 KB
english, 2010
Conversion to is in progress
Conversion to is failed