000 01230 a2200361 4500
005 20250517234715.0
264 0 _c20181114
008 201811s 0 0 eng d
022 _a1872-8464
024 7 _a10.1016/j.ijporl.2018.07.028
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMoassass, Faten
245 0 0 _aInvestigation of the mtDNA mutations in Syrian families with non-syndromic sensorineural hearing loss.
_h[electronic resource]
260 _bInternational journal of pediatric otorhinolaryngology
_cOct 2018
300 _a110-114 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAdolescent
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aDNA, Mitochondrial
_xgenetics
650 0 4 _aFemale
650 0 4 _aGenotype
650 0 4 _aHearing Loss, Sensorineural
_xgenetics
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aSyria
700 1 _aAl-Halabi, Bassel
700 1 _aNweder, Mohamad Sayah
700 1 _aAl-Achkar, Walid
773 0 _tInternational journal of pediatric otorhinolaryngology
_gvol. 113
_gp. 110-114
856 4 0 _uhttps://doi.org/10.1016/j.ijporl.2018.07.028
_zAvailable from publisher's website
999 _c28794944
_d28794944