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Q52877119-05A8A8B3-FC48-493A-B84F-1608057016A7
Q52877119-05A8A8B3-FC48-493A-B84F-1608057016A7
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http://www.wikidata.org/entity/statement/Q52877119-05A8A8B3-FC48-493A-B84F-1608057016A7
Novel mutations in the gene for α-subunit of retinal cone cyclic nucleotide-gated channels in a Japanese patient with congenital achromatopsia.
P2860
Q52877119-05A8A8B3-FC48-493A-B84F-1608057016A7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52877119-05A8A8B3-FC48-493A-B84F-1608057016A7
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e63241ed8bea64ec4285612802c67fdd2b4be52f
P2860
Whole-exome sequencing identifies ALMS1, IQCB1, CNGA3, and MYO7A mutations in patients with Leber congenital amaurosis.