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HUMU.9067
HUMU.9067
http://dx.doi.org/10.1002/HUMU.9067
Evidence of a founder effect for the RETGC1 (GUCY2D) 2943DelG mutation in Leber congenital amaurosis pedigrees of Finnish origin.
P356
Q44153681-58BDE077-8874-4EDB-B324-DBD68897C2C9
P356
HUMU.9067
http://dx.doi.org/10.1002/HUMU.9067