Identification of mutations in the MYO9A gene in patients with congenital myasthenic syndrome.
O'Connor E, Töpf A, Müller JS, Cox D, Evangelista T, Colomer J, Abicht A, Senderek J, Hasselmann O, Yaramis A, Laval SH, Lochmüller H.
O'Connor E, et al. Among authors: laval sh.
Brain. 2016 Aug;139(Pt 8):2143-53. doi: 10.1093/brain/aww130. Epub 2016 Jun 3.
Brain. 2016.
PMID: 27259756
Free PMC article.