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Q30357625-6660B088-D9CE-46F1-941C-50C16DB22624
Q30357625-6660B088-D9CE-46F1-941C-50C16DB22624
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30357625-6660B088-D9CE-46F1-941C-50C16DB22624
A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60
P2860
Q30357625-6660B088-D9CE-46F1-941C-50C16DB22624
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30357625-6660B088-D9CE-46F1-941C-50C16DB22624
rank
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type
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wasDerivedFrom
8df97ccec5174ee0da9cc07d4daaa02a597a6ce3
P2860
Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter