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Q54572793-019A1966-526C-422C-9279-5612050A7438
Q54572793-019A1966-526C-422C-9279-5612050A7438
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54572793-019A1966-526C-422C-9279-5612050A7438
Two Iranian families with a novel mutation in GJB2 causing autosomal dominant nonsyndromic hearing loss.
P2860
Q54572793-019A1966-526C-422C-9279-5612050A7438
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54572793-019A1966-526C-422C-9279-5612050A7438
rank
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type
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Statement
wasDerivedFrom
95dcd9ded52d32b0d6a919d5ea2704511d66e598
P2860
A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families.