✦ LIBER ✦
Contiguous deletion of the NDP, MAOA, MAOB, and EFHC2 genes in a patient with Norrie disease, severe psychomotor retardation and myoclonic epilepsy
✍ Scribed by L. Rodriguez-Revenga; I. Madrigal; L.S. Alkhalidi; L. Armengol; E. González; C. Badenas; X. Estivill; M. Milà
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 171 KB
- Volume
- 143A
- Category
- Article
- ISSN
- 1552-4825
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