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Q35637197-F7F68A6C-7450-4914-89F8-6F03DD0AB8C9
Q35637197-F7F68A6C-7450-4914-89F8-6F03DD0AB8C9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35637197-F7F68A6C-7450-4914-89F8-6F03DD0AB8C9
Lack of phenotypic effect of triallelic variation in SPATA7 in a family with Leber congenital amaurosis resulting from CRB1 mutations.
P2860
Q35637197-F7F68A6C-7450-4914-89F8-6F03DD0AB8C9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35637197-F7F68A6C-7450-4914-89F8-6F03DD0AB8C9
rank
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type
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Statement
wasDerivedFrom
f741a5ca85e8fd855ed3efd5ee4dd7bc96c8d46f
P2860
IQCB1 mutations in patients with leber congenital amaurosis.