POLG1 mutations and stroke like episodes: a distinct clinical entity rather than an atypical MELAS syndrome
<p>Abstract</p> <p>Background</p> <p><it>POLG1</it> mutations have been associated with MELAS-like phenotypes. However given several clinical differences it is unknown whether <it>POLG1</it> mutations are possible causes of MELAS or give raise to a distinct clinical and genetic entity, named <it>POL...
Kaydedildi:
| Asıl Yazarlar: | , , , , , , , , , , , , , |
|---|---|
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BMC
2013-01-01
|
| Seri Bilgileri: | BMC Neurology |
| Konular: | |
| Online Erişim: | http://www.biomedcentral.com/1471-2377/13/8 |
| Etiketler: |
Etiket eklenmemiş, İlk siz ekleyin!
|