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Q35112278-3DB10EC3-D0FD-4462-9223-09F78EA96D58
Q35112278-3DB10EC3-D0FD-4462-9223-09F78EA96D58
BestRank
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http://www.wikidata.org/entity/statement/Q35112278-3DB10EC3-D0FD-4462-9223-09F78EA96D58
Screening of a large cohort of leber congenital amaurosis and retinitis pigmentosa patients identifies novel LCA5 mutations and new genotype-phenotype correlations
P2860
Q35112278-3DB10EC3-D0FD-4462-9223-09F78EA96D58
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35112278-3DB10EC3-D0FD-4462-9223-09F78EA96D58
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wasDerivedFrom
cb270033d54bca4f2b49f2c70a915d76ceb6d30f
P2860
Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosis