| Autor: |
Kinga, Hadzsiev, Mónika, Szőts, Anett, Fekete, László, Balikó, Kim, Boycott, Ferenc, Nagy, Béla, Melegh |
| Rok vydání: |
2017 |
| Předmět: |
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| Zdroj: |
Orvosi hetilap. 158(42) |
| ISSN: |
0030-6002 |
| Popis: |
In a patient with marked symptoms of Huntington disease after the huntingtin testing, which gave normal result, a whole exome sequencing (WES) has been performed based on an international collaboration. A homozygous GA nucleotid change in the exon 34 of the VPS13A gene has been detected with WES, a mutation resulting in a premature stop codon at the position 1301. This change is a known pathogenic mutation. The aim of this article is to draw attention on the importance of the WES in the diagnosis of rare neurological diseases without any specific symptoms. Orv Hetil. 2017; 158(42): 1681-1684. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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