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

Yoel Hirsch, David A. Zeevi, Byron L. Lam, Sholem Y. Scher, Rachel Bringer, Bitya Cherki, Cadina C. Cohen, Hagit Muallem, John Chiang, Madhulatha Pantrangi, Josef Ekstein, Martin M. Johansson

Research output: Contribution to journal › Article › peer-review

2 Scopus citations

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Medicine & Life Sciences