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Q37359831-6EA1BCF7-B8EA-4143-ABCD-14BF13C3164A
Q37359831-6EA1BCF7-B8EA-4143-ABCD-14BF13C3164A
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http://www.wikidata.org/entity/statement/Q37359831-6EA1BCF7-B8EA-4143-ABCD-14BF13C3164A
Novel TRPM1 mutations in two Chinese families with early-onset high myopia, with or without complete congenital stationary night blindness.
P2860
Q37359831-6EA1BCF7-B8EA-4143-ABCD-14BF13C3164A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37359831-6EA1BCF7-B8EA-4143-ABCD-14BF13C3164A
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wasDerivedFrom
64ea06c5275250629a4ea64c84ef060baa230207
P2860
Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness