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Mutational screening in patients with profound sensorineura..:
Ammar, Marwa
;
Tabebi, Mouna
;
Sfaihi, Lamia
...
Biochemical and Biophysical Research Communications. 474 (2016) 4 - p. 702-708 , 2016
Link:
https://doi.org/10.1016/j.bbrc.2016.05.014
RT Journal T1 <Title>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</Title> UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.bbrc.2016.05.014&Exemplar=1&LAN=DE A1 Ammar, Marwa A1 Tabebi, Mouna A1 Sfaihi, Lamia A1 Alila-Fersi, Olfa A1 Maalej, Marwa A1 Felhi, Rahma A1 Chabchoub, Imen A1 Keskes, Leila A1 Hachicha, Mongia A1 Fakhfakh, Faiza A1 Mkaouar-Rebai, Emna PB Elsevier BV YR 2016 SN 0006-291X JF Biochemical and Biophysical Research Communications VO 474 IS 4 SP 702 OP 708 LK http://dx.doi.org/https://doi.org/10.1016/j.bbrc.2016.05.014 DO https://doi.org/10.1016/j.bbrc.2016.05.014 SF ELIB - SuUB Bremen
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