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Q30389304-09F606AD-6C48-458C-A068-E8581F20DDD9
Q30389304-09F606AD-6C48-458C-A068-E8581F20DDD9
BestRank
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http://www.wikidata.org/entity/statement/Q30389304-09F606AD-6C48-458C-A068-E8581F20DDD9
Homozygosity mapping and targeted sanger sequencing reveal genetic defects underlying inherited retinal disease in families from pakistan.
P2860
Q30389304-09F606AD-6C48-458C-A068-E8581F20DDD9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30389304-09F606AD-6C48-458C-A068-E8581F20DDD9
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Statement
wasDerivedFrom
39774a5a037375fb754d5743d255092e087fd335
P2860
Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis