טוען...
Episodic Ataxia Type 2 due to a Deletion Mutation in the CACNA1A Gene in a Korean Family
Episodic ataxia type 2 (EA-2) is an inherited disorder that is characterized by intermittent vertigo, ataxia, and interictal gaze-evoked nystagmus. Although abnormalities associated with this disorder have been found in the CACNA1A gene encoding the alpha1A (Cav2.1) subunit of the P/Q-type calcium c...
שמור ב:
| Main Authors: | , , , |
|---|---|
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Korean Neurological Association
2006
|
| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2854978/ https://ncbi.nlm.nih.gov/pubmed/20396531 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3988/jcn.2006.2.4.268 |
| תגים: |
הוספת תג
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!
|