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Q34404974-EC287866-03BF-4913-A987-DD5B0581AE0E
Q34404974-EC287866-03BF-4913-A987-DD5B0581AE0E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34404974-EC287866-03BF-4913-A987-DD5B0581AE0E
Advantage of Whole Exome Sequencing over Allele-Specific and Targeted Segment Sequencing in Detection of Novel TULP1 Mutation in Leber Congenital Amaurosis.
P921
Q34404974-EC287866-03BF-4913-A987-DD5B0581AE0E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34404974-EC287866-03BF-4913-A987-DD5B0581AE0E
rank
NormalRank
type
BestRank
Statement
P921
birth defect