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Clinical features in a large Iranian family with a limb-girdle congenital myasthenic syndrome due to a mutation in DPAGT1

✍ Scribed by Basiri, Keivan; Belaya, Katsiaryna; Liu, Wei Wei; Maxwell, Susan; Sedghi, Maryam; Beeson, David


Book ID
123489453
Publisher
Elsevier Science
Year
2013
Tongue
English
Weight
438 KB
Volume
23
Category
Article
ISSN
0960-8966

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