Clinical and molecular findings in eight Egyptian patients with suspected mitochondrial disorders and optic atrophy
By: Afat, Layla K.; al-Basyuni, Halah T.; Zaki, Maha S.…[et al.]. The Egyptian Journal of Medical Human Genetics. Vol. 14, no. 1 (Jan. 2013), pp.37-47, 11 p.
Subjects: Egypt; Diseases