A Novel Homozygous GRK1 Mutation (P391H) in 2 Siblings with...

A Novel Homozygous GRK1 Mutation (P391H) in 2 Siblings with Oguchi Disease with Markedly Reduced Cone Responses

Takaaki Hayashi, Tamaki Gekka, Tomokazu Takeuchi, Satoshi Goto-Omoto, Kenji Kitahara
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Volume:
114
Year:
2007
Language:
english
DOI:
10.1016/j.ophtha.2006.05.069
File:
PDF, 1.40 MB
english, 2007
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