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Mutations in FA2H in three Arab families with a clinical spectrum of neurodegeneration and hereditary spastic paraparesis.
- Source :
-
Clinical Genetics . Jul2015, Vol. 88 Issue 1, p95-97. 3p. 1 Diagram, 1 Chart. - Publication Year :
- 2015
-
Abstract
- A letter to the editor is presented concerning the fatty acid 2-hydroxylase (FA2H) gene mutation in three Arab families which developed neurodegeneration and hereditary spastic paraparesis.
- Subjects :
- *GENETIC mutation
*FAMILIES
*NEURODEGENERATION
Subjects
Details
- Language :
- English
- ISSN :
- 00099163
- Volume :
- 88
- Issue :
- 1
- Database :
- Academic Search Index
- Journal :
- Clinical Genetics
- Publication Type :
- Academic Journal
- Accession number :
- 103105440
- Full Text :
- https://doi.org/10.1111/cge.12516