Search Results - Zilbersztajn, Dinorah

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    Thomsen or Becker myotonia? A novel autosomal recessive nonsense mutation in the CLCN1 gene associated with a mild phenotype

    Thomsen or Becker myotonia? A novel autosomal recessive nonsense mutation in the CLCN1 gene associated with a mild phenotype by Gurgel‐Giannetti, Juliana, Senkevics, Adriano S., Zilbersztajn‐Gotlieb, Dinorah, Yamamoto, Lydia U., Muniz, Viviane P., Pavanello, Rita C.M., Oliveira, Acary B., ZATZ, Mayana, Vainzof, Mariz

    Published in Muscle & nerve
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    Genetic variability in the myostatin gene does not explain the muscle hypertrophy and clinical penetrance in myotonia congenita

    Genetic variability in the myostatin gene does not explain the muscle hypertrophy and clinical penetrance in myotonia congenita by Muniz, Viviane P., Senkevics, Adriano S., Zilbersztajn, Dinorah, Gurgel-Giannetti, Juliana, Silva, Helga C., Yamamoto, Lydia U., Pavanello, Rita C.M., Pearson, Peter L., Zatz, Mayana, Vainzof, Mariz

    Published in Muscle & nerve
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    Thomsen or Becker myotonia? A novel autosomal recessive nonsense mutation in the CLCN1 gene associated with a mild phenotype

    Thomsen or Becker myotonia? A novel autosomal recessive nonsense mutation in the CLCN1 gene associated with a mild phenotype by Gurgel-Giannetti, Juliana, Senkevics, Adriano S., Zilbersztajn-Gotlieb, Dinorah, Yamamoto, Lydia U., Muniz, Viviane P., Pavanello, Rita C.M., Oliveira, Acary B., ZATZ, Mayana, Vainzof, Mariz

    Published in Muscle & Nerve
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