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Q33722973-B31F91A9-CCE9-45E6-BE61-83450A17130E
Q33722973-B31F91A9-CCE9-45E6-BE61-83450A17130E
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http://www.wikidata.org/entity/statement/Q33722973-B31F91A9-CCE9-45E6-BE61-83450A17130E
Phenotype-genotype correlation with Sanger sequencing identified retinol dehydrogenase 12 (RDH12) compound heterozygous variants in a Chinese family with Leber congenital amaurosis.
P2860
Q33722973-B31F91A9-CCE9-45E6-BE61-83450A17130E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33722973-B31F91A9-CCE9-45E6-BE61-83450A17130E
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wasDerivedFrom
6245cff18ec8ae6a9716fc5e704cb74a7a53df49
P2860
IQCB1 mutations in patients with leber congenital amaurosis.