Inherited disorders of sarcomeric proteins

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20 Citations (Scopus)


The most important advances in sarcomeric protein diseases continue to be the identification of mutated genes responsible for human diseases. These have recently included those that encode skeletal muscle alpha-actin in autosomal dominant and autosomal recessive nemaline myopathy, nebulin and slow alpha-tropomyosin in autosomal recessive nemaline myopathy, and desmin and alpha B-crystallin in desminopathies. Curr Opin Neurol 12:513-518 (C) 1999 Lippincott Williams & Wilkins.
Original languageEnglish
Pages (from-to)513-518
JournalCurrent Opinion in Neurology
Publication statusPublished - 1999


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