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  • Edoardo Malfatti, Ursula Schaeffer, Françoise Chapon, Yage Yang, Norma Beatriz Romero
  • Medicine, Biology
  • Neuromuscular Disorders
  • 2013 (First Publication: 1 October 2013)
  • The slow α-tropomyosin gene (TPM3) has been associated with three distinct histological entities: nemaline myopathy (NM, NEM1), congenital fibre-type disproportion (CFTD), and cap disease (CD). HereExpand