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Neonatal vocal cord paralysis-an early presentation of hereditary neuralgic amyotrophy due to a mutation in the SEPT9 gene

✍ Scribed by Leshinsky-Silver, E.; Ginzberg, M.; Dabby, R.; Sadeh, M.; Lev, D.; Lerman-Sagie, T.


Book ID
121503419
Publisher
Elsevier Science
Year
2013
Tongue
English
Weight
346 KB
Volume
17
Category
Article
ISSN
1090-3798

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