A novel HAX1 gene mutation in severe congenital neutropenia (SCN) associated with neurological manifestations.
| Autor: | Faiyaz-Ul-Haque, Muhammad1,2 MFHaque@Kfshrc.edu.sa, Al-Jefri, Abdullah3, Al-Dayel, Fouad1, Bhuiyan, Jalaluddin A. K. M.1, Abalkhail, Hala A.1, Al-Nounou, Randa1, Al-Abdullatif, Ahmed1, Pulicat, Monogaran S.4, Gaafar, Ameera4, Alaiya, Ayodele A.4, Peltekova, Iskra5, Zaidi, Syed H. E.6 Syed.Zaidi@uhnres.utoronto.ca |
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| Zdroj: | European Journal of Pediatrics. Jun2010, Vol. 169 Issue 6, p661-666. 6p. 1 Diagram, 1 Graph. |
| Databáze: | Academic Search Ultimate |
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