- Tytuł:
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Contiguous deletion of the NDP, MAOA, MAOB, and EFHC2 genes in a patient with Norrie disease, severe psychomotor retardation and myoclonic epilepsyHow to cite this article: Rodriguez‐Revenga L, Madrigal I, Alkhalidi LS, Armengol L, González E, Badenas C,
Estivill X , Milà M. 2007. Contiguous deletion of the NDP, MAOA, MAOB, and EFHC2 genes in a patient with Norrie disease, severe psychomotor retardation and myoclonic epilepsy. Am J Med Genet Part A 143A:916–920. - Autorzy:
- Źródło:
- American Journal of Medical Genetics. Part A; May 2007, Vol. 143 Issue: 9 p916-920, 5p
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