Clinical and molecular findings in eight Egyptian patients with suspected mitochondrial disorders and optic atrophy
Al-Ettribi, Ghada M.M., Effat, Laila K., El-Bassyouni, Hala T., Zaki, Maha S., Shanab, Gamila, Karim, Amr M.Volume:
14
Language:
english
Journal:
Egyptian Journal of Medical Human Genetics
DOI:
10.1016/j.ejmhg.2012.08.002
Date:
January, 2013
File:
PDF, 1.38 MB
english, 2013