LOC115925415 Literature

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Echinobase

Summary

Expression

Gene Literature (1447)

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, Ocaña-Sierra J, Calzolari E, Cambiaghi S, Scudder PM, Hovnanian A, Monaco AP, Munro CS., Hum Mol Genet. July 1, 1999; 8 (7): 1237-43.

A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel''s syndrome) in three unrelated families., Maestrini E, Korge BP, Ocaña-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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