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Q41197627-17EC4586-5474-49F5-B0FC-FFD9D19174E1
Q41197627-17EC4586-5474-49F5-B0FC-FFD9D19174E1
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http://www.wikidata.org/entity/statement/Q41197627-17EC4586-5474-49F5-B0FC-FFD9D19174E1
Carrier re-sequencing reveals rare but benign variants in recessive deafness genes.
P2860
Q41197627-17EC4586-5474-49F5-B0FC-FFD9D19174E1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41197627-17EC4586-5474-49F5-B0FC-FFD9D19174E1
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7bd51ecc4f43568a28eca3274c1109ae62887c50
P2860
Clinical features of patients with GJB2 (connexin 26) mutations: severity of hearing loss is correlated with genotypes and protein expression patterns.