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Clin Genet. 2015 Jul;88(1):95-7. doi: 10.1111/cge.12516. Epub 2014 Dec 11.

Mutations in FA2H in three Arab families with a clinical spectrum of neurodegeneration and hereditary spastic paraparesis.

Author information

1
Clinical Genetics Department, National Research Centre, Cairo, Egypt.
2
Pediatric Neurology Department, Cairo University, Cairo, Egypt.
3
Neurogenetics Laboratory, Department of Neurosciences, Howard Hughes Medical Institute, University of California, San Diego, CA, USA.
4
Broad Institute of Harvard and Massachusetts Institute of Technology, Cambridge, MA, USA.
PMID:
25496456
DOI:
10.1111/cge.12516
[Indexed for MEDLINE]

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