Neonatal vocal cord paralysis-an early presentation of hereditary neuralgic amyotrophy due to a mutation in the SEPT9 gene
Leshinsky-Silver, E., Ginzberg, M., Dabby, R., Sadeh, M., Lev, D., Lerman-Sagie, T.Volume:
17
Language:
english
Journal:
European Journal of Paediatric Neurology
DOI:
10.1016/j.ejpn.2012.08.006
Date:
January, 2013
File:
PDF, 346 KB
english, 2013