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1
Q36202202-82892FC3-CEFE-43CF-A6E8-5D5E5F971A0B
Q36202202-82892FC3-CEFE-43CF-A6E8-5D5E5F971A0B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36202202-82892FC3-CEFE-43CF-A6E8-5D5E5F971A0B
Identification of novel mutations by targeted exome sequencing and the genotype-phenotype assessment of patients with achromatopsia.
P2860
Q36202202-82892FC3-CEFE-43CF-A6E8-5D5E5F971A0B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36202202-82892FC3-CEFE-43CF-A6E8-5D5E5F971A0B
rank
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type
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Statement
wasDerivedFrom
7e7b42a7e5e5fb3ff38b75897d9610b765fed3df
P2860
Homozygous missense variant in the human CNGA3 channel causes cone-rod dystrophy