Contiguous deletion of the NDP, MAOA, MAOB, and EFHC2 genes in a patient with Norrie disease, severe psychomotor retardation and myoclonic epilepsy.
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| Description | scientific article |
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author: Celia Badenas Eva Gonzalez-Roca Irene Madrigal Montserrat Milà Xavier Estivill i Pallejà |
| Publication date | May 1, 2007 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |