TY - JOUR PY - 2016 J2 - Biochem. Biophys. Res. Commun. SN - 0006-291X T2 - Biochemical and Biophysical Research Communications VL - 474 IS - 4 DO - 10.1016/j.bbrc.2016.05.014 TI - Mutational screening in patients with profound sensorineural hearing loss and neurodevelopmental delay: Description of a novel m.3861A > C mitochondrial mutation in the MT-ND1 gene UR - https://www.cheric.org/research/tech/periodicals/view.php?seq=1465984 KW - Mitochondrial mutations KW - mtDNA KW - MT-ND1 KW - m.3861A > C KW - Hearing loss AU - Ammar M AU - Tabebi M AU - Sfaihi L AU - Alila-Fersi O AU - Maalej M AU - Felhi R AU - Chabchoub I AU - Keskes L AU - Hachicha M AU - Fakhfakh F AU - Mkaouar-Rebai E SP - 702 EP - 708 LA - English ER -