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Clinical and Molecular Analysis of a Novel COLQ Missense Mutation Causing Congenital Myasthenic Syndrome in a Syrian Family

✍ Scribed by Matlik, Hussein N.; Milhem, Reham M.; Saadeldin, Imad Y.; Al-Jaibeji, Hayat S.; Al-Gazali, Lihadh; Ali, Bassam R.

Book ID: 122211770
Publisher: Elsevier Science
Year: 2014
Tongue: English
Weight: 432 KB
Volume: 51
Category: Article
ISSN: 0887-8994
DOI: 10.1016/j.pediatrneurol.2014.03.012

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