Novel missense mutation in the ATP1A2 gene associated with atypical sporadic hemiplegic migraine

Hemiplegic migraine (HM) is a rare subtype of migraine with aura in which attacks include transient motor weakness or hemiparesis that can last several days. HM is linked to mutations in three different genes, CACNA1A, ATP1A2 and SCN1A, which encode for ion transporters. The clinical spectrum includ...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:BMJ Case Rep
Asıl Yazarlar: Rispoli, Marianna Gabriella, Di Stefano, Vincenzo, Mantuano, Elide, De Angelis, Maria Vittoria
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BMJ Publishing Group 2019
Konular:
Rare Disease
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6781968/
https://ncbi.nlm.nih.gov/pubmed/31586957
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2019-231129
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller