G59S mutation in the GJB2 (connexin 26) gen... [Am J Med Genet A. 2005] - PubMed

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Expanding the phenotypic spectrum of Cx26 disorders: Bart-Pumphrey syndrome is caused by a novel missense mutation in GJB2. [J Invest Dermatol. 2004]
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Cited by 3 PubMed Central articles

GJB2 Gene Mutations in Syndromic Skin Diseases with Sensorineural Hearing Loss. [Curr Genomics. 2011]
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G59S mutation in the GJB2 (connexin 26) gene in a patient with Bart-Pumphrey syn...
G59S mutation in the GJB2 (connexin 26) gene in a patient with Bart-Pumphrey syndrome.
Am J Med Genet A. 2005 Jul 30 ;136(3):282-4.

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