Mutations in FA2H in three Arab...

Clinical Genetics 2015 / 07 Vol. 88; Iss. 1

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

Zaki, M. S., Selim, L., Mansour, L., Mahmoud, I. G., Fenstermaker, A. G., Gabriel, S. B., Gleeson, J. G.
How much do you like this book?
What’s the quality of the file?
Download the book for quality assessment
What’s the quality of the downloaded files?
Volume:
88
Language:
english
Journal:
Clinical Genetics
DOI:
10.1111/cge.12516
Date:
July, 2015
File:
PDF, 320 KB
english, 2015
Conversion to is in progress
Conversion to is failed