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Mutation in the gene for connexin 30.3 in a family with erythrokeratodermia variabilis.
Macari, F; Landau, M; Cousin, P; Mevorah, B; Brenner, S; Panizzon, R; Schorderet, D F; Hohl, D; Huber, M.
Affiliation
  • Macari F; Department of Dermatology, University Hospital, CH-1011 Lausanne, Switzerland.
Am J Hum Genet ; 67(5): 1296-301, 2000 Nov.
Article in En | MEDLINE | ID: mdl-11017804

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 1 / Connexins / Genetic Heterogeneity / Mutation, Missense / Erythema Limits: Adult / Child / Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Am J Hum Genet Year: 2000 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 1 / Connexins / Genetic Heterogeneity / Mutation, Missense / Erythema Limits: Adult / Child / Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Am J Hum Genet Year: 2000 Document type: Article