| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8689203 | Neurología Argentina | 2018 | 10 Pages |
Abstract
The molecular diagnosis of point mutations through massively parallel sequencing allowed to reach the diagnostic confirmation efficiently, defining for the negative cases for deletion/duplication, the adequate advice and the implementation of appropriate therapeutic management.
Keywords
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Authors
Mary GarcÃa-Acero, Tatiana Pineda, Mariana Guerra-Torres, Reggie GarcÃa-Robles, Paola Ayala-RamÃrez, Tatiana Buitrago, Alisson Poveda, Fernando Suárez-Obando,