A novel p.Gly603Arg mutation in CACNA1F causes Åland island eye disease and incomplete congenital stationary night blindness phenotypes in a family
| Main Authors: | , , , , |
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| Format: | Online |
| Language: | English |
| Published: |
Molecular Vision
2011
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3244487/ |