Mild phenotype of nemaline myopathy with sleep hypoventilation due to a mutation in the skeletal muscle α-actin (ACTA1) gene

✍ Scribed by H Jungbluth; C.A Sewry; S.C Brown; K.J Nowak; N.G Laing; C Wallgren-Pettersson; K Pelin; A.Y Manzur; E Mercuri; V Dubowitz; F Muntoni

• Book ID: 117669350
• Publisher: Elsevier Science
• Year: 2001
• Tongue: English
• Weight: 893 KB
• Volume: 11
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/s0960-8966(00)00167-x