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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

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Academic year: 2020

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Figure

Fig. 1. Pedigree and SSCP analysis of the Costa Rican family with Becker disease. (A) Pedigree of the family affected by  Becker disease
Fig.  2.  Sequence  analysis  of  exon  11  region  where  the  new  mutation  is  located
Fig.  4. Alignment  of  the  CLC-1  chloride  channel  among  different  species  in  the  region  of  the  exon  11  mutation

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