DOI:
10.1055/s-00000031
Klinische Monatsblätter für Augenheilkunde
LinksClose Window
References
Bech-Hansen NT, Naylor MJ, Maybaum TA. et al.
Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness.
Nat Genet 1998;
19: 264-267
Search in:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.