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Q28262677-3A5A44BE-5C57-4856-BD01-93C75C4F3E69
Q28262677-3A5A44BE-5C57-4856-BD01-93C75C4F3E69
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28262677-3A5A44BE-5C57-4856-BD01-93C75C4F3E69
Compound heterozygous CNGA3 mutations (R436W, L633P) in a Japanese patient with congenital achromatopsia
P2860
Q28262677-3A5A44BE-5C57-4856-BD01-93C75C4F3E69
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28262677-3A5A44BE-5C57-4856-BD01-93C75C4F3E69
rank
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type
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Statement
wasDerivedFrom
c73d5507d60081b74ae4875fe7bff39961d22caa
P2860
CNGA3 mutations in hereditary cone photoreceptor disorders