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Q41929730-3BC1239F-20D1-4044-902D-9260E1AF14B3
Q41929730-3BC1239F-20D1-4044-902D-9260E1AF14B3
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http://www.wikidata.org/entity/statement/Q41929730-3BC1239F-20D1-4044-902D-9260E1AF14B3
Value of whole exome sequencing for syndromic retinal dystrophy diagnosis in young patients.
P2860
Q41929730-3BC1239F-20D1-4044-902D-9260E1AF14B3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41929730-3BC1239F-20D1-4044-902D-9260E1AF14B3
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bb26bfcb796d448324d277b27b2205816198db9f
P2860
Advantage of Whole Exome Sequencing over Allele-Specific and Targeted Segment Sequencing in Detection of Novel TULP1 Mutation in Leber Congenital Amaurosis.