טוען...
Late-onset Huntington’s disease with 40–42 CAG expansion
INTRODUCTION: Huntington’s disease (HD) is a rare autosomal dominant neurodegenerative disorder caused by a CAG expansion greater than 35 in the IT-15 gene. There is an inverse correlation between the number of pathological CAG and the age of onset. However, CAG repeats between 40 and 42 showed a wi...
שמור ב:
| הוצא לאור ב: | Neurol Sci |
|---|---|
| Main Authors: | , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Springer International Publishing
2019
|
| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7160095/ https://ncbi.nlm.nih.gov/pubmed/31820322 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10072-019-04177-8 |
| תגים: |
הוספת תג
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!
|