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Mutations in FA2H in three Arab families with a clinical spectrum of neurodegeneration and hereditary spastic paraparesis.
- Source :
-
Clinical genetics [Clin Genet] 2015 Jul; Vol. 88 (1), pp. 95-7. Date of Electronic Publication: 2014 Dec 11. - Publication Year :
- 2015
- Subjects :
- Adolescent
Arabs genetics
Child
Child, Preschool
DNA Mutational Analysis
Female
Homozygote
Humans
Male
Neurodegenerative Diseases diagnosis
Paraparesis, Spastic diagnosis
Pedigree
Phenotype
Mixed Function Oxygenases genetics
Mutation
Neurodegenerative Diseases genetics
Paraparesis, Spastic genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1399-0004
- Volume :
- 88
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Clinical genetics
- Publication Type :
- Report
- Accession number :
- 25496456
- Full Text :
- https://doi.org/10.1111/cge.12516