A Novel Mutation in the Mitochondrial DNA Cytochrome b Gene (MTCYB) in a Patient with Prader Willi Syndrome
Yi , U., Ezgu, F. S., Karakaya, P., Polat, I., Arslan, N., Cankaya, T., Bozkaya, O. G., Kurul, S. H.Volume:
30
Language:
english
Journal:
Journal of Child Neurology
DOI:
10.1177/0883073814530499
Date:
March, 2015
File:
PDF, 368 KB
english, 2015