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Q34784703-69A3B085-3E70-4496-9662-426304534CCB
Q34784703-69A3B085-3E70-4496-9662-426304534CCB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34784703-69A3B085-3E70-4496-9662-426304534CCB
Exome sequencing reveals novel and recurrent mutations with clinical significance in inherited retinal dystrophies
P2860
Q34784703-69A3B085-3E70-4496-9662-426304534CCB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34784703-69A3B085-3E70-4496-9662-426304534CCB
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wasDerivedFrom
f85ba3045ad22598c9199d207ff4036368482f57
P2860
Whole-exome sequencing identifies novel compound heterozygous mutations in USH2A in Spanish patients with autosomal recessive retinitis pigmentosa