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Novel COLQ mutation 950delC in synaptic congenital myasthenic syndrome and symptomatic heterozygous relatives

✍ Scribed by Felix Schreiner; Marc Hoppenz; Ruth Klaeren; Jens Reimann; Joachim Woelfle


Book ID
116792783
Publisher
Elsevier Science
Year
2007
Tongue
English
Weight
296 KB
Volume
17
Category
Article
ISSN
0960-8966

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