Two familial cases of Olmsted-like syndrome with a G573V mutation of the TRPV3 gene.

Zhi, Y P; Liu, J; Han, J W; Huang, Y P; Gao, Z Q; Yang, Y; Wu, R N

Zhi, Y P; Liu, J; Han, J W; Huang, Y P; Gao, Z Q; Yang, Y; Wu, R N.

Afiliación

Zhi YP; Department of Dermatology, International Mongolian Hospital of Inner Mongolia, Hohhot, Inner Mongolia Autonomous Region, PR China.
Liu J; Department of Dermatology, Affiliated Hospital of Inner Mongolia Medical University, Hohhot, Inner Mongolia Autonomous Region, PR China.
Han JW; Department of Dermatology, Affiliated Hospital of Inner Mongolia Medical University, Hohhot, Inner Mongolia Autonomous Region, PR China.
Huang YP; Department of Dermatology, Affiliated Hospital of Inner Mongolia Medical University, Hohhot, Inner Mongolia Autonomous Region, PR China.
Gao ZQ; Department of Dermatology, International Mongolian Hospital of Inner Mongolia, Hohhot, Inner Mongolia Autonomous Region, PR China.
Yang Y; Department of Dermatology, Peking University First Hospital, Beijing, PR China.
Wu RN; Department of Dermatology, International Mongolian Hospital of Inner Mongolia, Hohhot, Inner Mongolia Autonomous Region, PR China.

Clin Exp Dermatol ; 41(5): 510-3, 2016 Jul.

Article en En | MEDLINE | ID: mdl-27273692

Asunto(s)

Predisposición Genética a la Enfermedad/genética; Queratodermia Palmoplantar/genética; Mutación Missense; Canales Catiónicos TRPV/genética; Adulto; Preescolar; Femenino; Humanos; Masculino; Síndrome

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Queratodermia Palmoplantar / Predisposición Genética a la Enfermedad / Mutación Missense / Canales Catiónicos TRPV Tipo de estudio: Prognostic_studies Límite: Adult / Child, preschool / Female / Humans / Male Idioma: En Revista: Clin Exp Dermatol Año: 2016 Tipo del documento: Article Pais de publicación: Reino Unido

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