First familial Becker muscular dystrophy in Tanzania: Clinical and genetic features<sup>.</sup>

Dekker, M C J; Tieleman, A A; Igogo, O J; van Duyvenvoorde, H A; Howlett, W P; Hamel, B C

First familial Becker muscular dystrophy in Tanzania: Clinical and genetic features^.

Dekker, M C J; Tieleman, A A; Igogo, O J; van Duyvenvoorde, H A; Howlett, W P; Hamel, B C.

Afiliación

Dekker MCJ; Departments of Medicine and Urology, Kilimanjaro Christian Medical Centre, P.O. Box 3010, Moshi, Kilimanjaro, Tanzania. Electronic address: marieke@zwets.com.
Tieleman AA; Department of Neurology, Radboud University Medical Centre, Nijmegen, The Netherlands.
Igogo OJ; Departments of Medicine and Urology, Kilimanjaro Christian Medical Centre, P.O. Box 3010, Moshi, Kilimanjaro, Tanzania.
van Duyvenvoorde HA; Department of Human Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
Howlett WP; Departments of Medicine and Urology, Kilimanjaro Christian Medical Centre, P.O. Box 3010, Moshi, Kilimanjaro, Tanzania.
Hamel BC; Department of Human Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands.

Neuromuscul Disord ; 29(4): 317-320, 2019 04.

Article en En | MEDLINE | ID: mdl-30926200

Asunto(s)

Distrofia Muscular de Duchenne; Humanos; Masculino; Persona de Mediana Edad; Distrofia Muscular de Duchenne/diagnóstico; Distrofia Muscular de Duchenne/genética; Distrofia Muscular de Duchenne/fisiopatología; Linaje; Tanzanía

Palabras clave

Africa; Becker muscular dystrophy; Global neurology; Muscular dystrophy

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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Distrofia Muscular de Duchenne Tipo de estudio: Diagnostic_studies Límite: Humans / Male / Middle aged País/Región como asunto: Africa Idioma: En Revista: Neuromuscul Disord Asunto de la revista: NEUROLOGIA Año: 2019 Tipo del documento: Article

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