טוען...
Case report and literature review of Huntington disease with intermediate CAG expansion
BACKGROUND: Huntington disease (HD) is a genetically inherited neurodegenerative disorder that classically involves a trinucleotide CAG repeat expansion on chromosome 4, with 36 repeats or greater being disease identifying. It generally presents between the age of 30 and 40 years old and is characte...
שמור ב:
| הוצא לאור ב: | BMJ Neurol Open |
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| Main Authors: | , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
BMJ Publishing Group
2020
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7871728/ https://ncbi.nlm.nih.gov/pubmed/33681777 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bmjno-2019-000027 |
| תגים: |
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