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Q26770321-F3B39433-5D35-496C-B3ED-923147AAC7AB
Q26770321-F3B39433-5D35-496C-B3ED-923147AAC7AB
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http://www.wikidata.org/entity/statement/Q26770321-F3B39433-5D35-496C-B3ED-923147AAC7AB
Retinal dystrophies, genomic applications in diagnosis and prospects for therapy
P2860
Q26770321-F3B39433-5D35-496C-B3ED-923147AAC7AB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q26770321-F3B39433-5D35-496C-B3ED-923147AAC7AB
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wasDerivedFrom
8a8feaf944fcbf12ad993792f4e65a52f8d4a358
P2860
Advantage of Whole Exome Sequencing over Allele-Specific and Targeted Segment Sequencing in Detection of Novel TULP1 Mutation in Leber Congenital Amaurosis.