Hypothyroidism could be the only manifestation of mitochondrial T8993C mutation in Leigh syndrome
By: Tammum, Huda; al-Sayyid, Sulaf; Kravis, Elizabeth Berry. The Egyptian Journal of Medical Human Genetics. Vol. 14, no. 2 (Apr. 2013), pp.201-203, 3 p.
Subjects: Egypt; Diseases; Thyroid gland