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ECB--23093569
Papers associated with LOC115925415 (and LOC100889396)
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A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel''s syndrome) in three unrelated families., Maestrini E, Korge BP, OcaƱa-Sierra J, Calzolari E, Cambiaghi S, Scudder PM, Hovnanian A, Monaco AP, Munro CS., Hum Mol Genet. July 1, 1999; 8 (7): 1237-43. |
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