CAV3 gene sequence variations: National Genome Database and clinics.

Stavusis, J; Inashkina, I; Jankevics, E; Radovica, I; Micule, I; Strautmanis, J; Naudina, M S; Utkus, A; Burnyte, B; Lace, B

Stavusis, J; Inashkina, I; Jankevics, E; Radovica, I; Micule, I; Strautmanis, J; Naudina, M S; Utkus, A; Burnyte, B; Lace, B.

Afiliación

Stavusis J; Latvian Biomedical Research and Study Center, Riga, Latvia.
Inashkina I; Latvian Biomedical Research and Study Center, Riga, Latvia.
Jankevics E; Latvian Biomedical Research and Study Center, Riga, Latvia.
Radovica I; Latvian Biomedical Research and Study Center, Riga, Latvia.
Micule I; Latvian Biomedical Research and Study Center, Riga, Latvia.
Strautmanis J; Latvian Biomedical Research and Study Center, Riga, Latvia.
Naudina MS; Latvian Biomedical Research and Study Center, Riga, Latvia.
Utkus A; Department of Human and Medical Genetics, Faculty of Medicine, Vilnius University, Vilnius, Lithuania.
Burnyte B; Centre for Medical Genetics, Vilnius University Hospital Santariskiu Klinikos, Vilnius, Lithuania.
Lace B; Department of Human and Medical Genetics, Faculty of Medicine, Vilnius University, Vilnius, Lithuania.

Acta Neurol Scand ; 132(3): 185-90, 2015 Sep.

Article en En | MEDLINE | ID: mdl-25630502

Asunto(s)

Caveolina 3/genética; Enfermedades Neuromusculares/genética; Adulto; Cardiomiopatías/genética; Creatina Quinasa/sangre; Femenino; Humanos; Masculino; Persona de Mediana Edad; Distrofia Muscular de Cinturas/genética; Mutación

Palabras clave

CAV3; LGMD1C; cardiomyopathy; caveolinopathy; hyperCKemia

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Caveolina 3 / Enfermedades Neuromusculares Tipo de estudio: Prognostic_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Acta Neurol Scand Año: 2015 Tipo del documento: Article País de afiliación: Letonia Pais de publicación: Dinamarca

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