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Clinical variability of CMS-EA (congenital myasthenic syndrome with episodic apnea) due to identical CHAT mutations in two infants

✍ Scribed by N. Barisic; J.S. Müller; E. Paucic-Kirincic; M. Gazdik; K. Lah-Tomulic; A. Pertl; J. Sertic; N. Zurak; H. Lochmüller; A. Abicht


Book ID
113590023
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
163 KB
Volume
9
Category
Article
ISSN
1090-3798

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