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P23.6 Congenital myasthenic syndrome with episodic apnea in a female infant caused by two different compound heterozygous mutations of the CHAT-gene

✍ Scribed by A. Sasso; K. Lah-Tomulic


Book ID
114360678
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
35 KB
Volume
15
Category
Article
ISSN
1090-3798

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