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A novel p.Gly603Arg mutation in CACNA1F causes Åland island eye disease and incomplete congenital stationary night blindness phenotypes in a family

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Description scientific article published on December 15, 2011
Author/s

author: Elise Héon  Ajoy Vincent  Thomas Wright 

Publication date December 15, 2011
Language English
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https://europepmc.org/articles/PMC3244487

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