Clinical and molecular diagnosis of a Costa Rican family with autosomal recessive myotonia congenita (Becker disease) carrying a new mutation in the CLCN1 gene. (Q54524754)
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English | Clinical and molecular diagnosis of a Costa Rican family with autosomal recessive myotonia congenita (Becker disease) carrying a new mutation in the CLCN1 gene. |
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Clinical and molecular diagnosis of a Costa Rican family with autosomal recessive myotonia congenita (Becker disease) carrying a new mutation in the CLCN1 gene (English)
Fernando Morales
Patricia Cuenca
Gerardo del Valle
Melissa Vásquez
Roberto Brian
Mauricio Sittenfeld
Keith Johnson
Xi Lin