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Q37618639-D136C709-1004-4996-9A6E-58DD750A6EFE
Q37618639-D136C709-1004-4996-9A6E-58DD750A6EFE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37618639-D136C709-1004-4996-9A6E-58DD750A6EFE
Whole-exome sequencing identifies ALMS1, IQCB1, CNGA3, and MYO7A mutations in patients with Leber congenital amaurosis.
P2860
Q37618639-D136C709-1004-4996-9A6E-58DD750A6EFE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37618639-D136C709-1004-4996-9A6E-58DD750A6EFE
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wasDerivedFrom
db6007201c6f3ddc9f3ad247939da0f8e917df92
P2860
IQCB1 mutations in patients with leber congenital amaurosis.