Faculty Opinions recommendation of Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain.
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2015 ◽
Vol 97
(6)
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pp. 878-885
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2018 ◽
Vol 28
(10)
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pp. 881-884
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