A1 Refereed original research article in a scientific journal
Clinically variable nemaline myopathy in a three-generation family caused by mutation of the skeletal muscle alpha-actin gene
Authors: Vilma-Lotta Lehtokari, Maria Gardberg, Katarina Pelin, Carina Wallgren-Pettersson
Publisher: Elsevier Ltd
Publication year: 2018
Journal: Neuromuscular Disorders
Journal name in source: Neuromuscular Disorders
Volume: 28
Issue: 4
First page : 323
Last page: 326
Number of pages: 4
ISSN: 0960-8966
eISSN: 1873-2364
DOI: https://doi.org/10.1016/j.nmd.2017.12.009
Self-archived copy’s web address: https://research.utu.fi/converis/portal/detail/Publication/30792900
Downloadable publication This is an electronic reprint of the original article. |