Clinically variable nemaline myopathy in a three-generation family caused by mutation of the skeletal muscle alpha-actin gene

: Vilma-Lotta Lehtokari, Maria Gardberg, Katarina Pelin, Carina Wallgren-Pettersson

Publisher: Elsevier Ltd

: 2018

: Neuromuscular Disorders

: Neuromuscular Disorders

: 28

: 4

: 323

: 326

: 4

: 0960-8966

: 1873-2364

DOI: https://doi.org/10.1016/j.nmd.2017.12.009

: https://research.utu.fi/converis/portal/detail/Publication/30792900