A founder deletion in the TRPM1 gene associated with...

Human Genome Variation 2019 / 12 Vol. 6; Iss. 1

A founder deletion in the TRPM1 gene associated with congenital stationary night blindness and myopia is highly prevalent in Ashkenazi Jews

Hirsch, Yoel, Zeevi, David A., Lam, Byron L., Scher, Sholem Y., Bringer, Rachel, Cherki, Bitya, Cohen, Cadina C., Muallem, Hagit, Chiang, John (Pei-Wen), Pantrangi, Madhulatha, Ekstein, Josef, Johanss
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:
6
Journal:
Human Genome Variation
DOI:
10.1038/s41439-019-0076-4
Date:
December, 2019
File:
PDF, 671 KB
2019
Conversion to is in progress
Conversion to is failed