Author:
Salih Mustafa A. M.,Kang Peter B.
Publisher
Springer International Publishing
Reference24 articles.
1. Salih MA. Neuromuscular transmission disorders. In: Textbook of clinical pediatrics. Berlin: Springer; 2012. p. 3493–3502.
2. Engel AG, Shen XM, Selcen D, Sine SM. Congenital myasthenic syndromes: pathogenesis, diagnosis, and treatment. Lancet Neurol. 2015;14(4):420–34.
3. Abicht A, Müller J S, Lochmüller H. Congenital myasthenic syndromes. 2003 May 9 [Updated 2016 Jul 14]. In: Pagon RA, Adam MP, Ardinger HH, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2016.
http://www.ncbi.nlm.nih.gov/books/NBK1168/
4. Ravenscroft G, Davis MR, Lamont P, Forrest A, Laing NG. New era in genetics of early-onset muscle disease: breakthroughs and challenges. In: Seminars in cell & developmental biology. Academic Press; 2016.
5. Mihaylova V, Müller JS, Vilchez JJ, Salih MA, Kabiraj MM, D’Amico A, et al. Clinical and molecular genetic findings in COLQ-mutant congenital myasthenic syndromes. Brain. 2008;131(3):747–59.