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Q50436454-2A4E8EB7-B1C1-4073-BE4E-99DF7E252A37
Q50436454-2A4E8EB7-B1C1-4073-BE4E-99DF7E252A37
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http://www.wikidata.org/entity/statement/Q50436454-2A4E8EB7-B1C1-4073-BE4E-99DF7E252A37
Impaired membrane targeting and aberrant cellular localization of human Cx26 mutants associated with inherited recessive hearing loss.
P2860
Q50436454-2A4E8EB7-B1C1-4073-BE4E-99DF7E252A37
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50436454-2A4E8EB7-B1C1-4073-BE4E-99DF7E252A37
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wasDerivedFrom
8c6cca5868c7ee69f940bbad366df10b90350aca
P2860
Autosomal recessive non-syndromic hearing loss in the Lebanese population: prevalence of the 30delG mutation and report of two novel mutations in the connexin 26 (GJB2) gene.