A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants
- 1 March 2001
- journal article
- research article
- Published by Springer Science and Business Media LLC in Human Genetics
- Vol. 108 (2), 91-97
- https://doi.org/10.1007/s004390100461