000 01581 a2200505 4500
005 20250518074443.0
264 0 _c20200529
008 202005s 0 0 eng d
022 _a2148-3817
024 7 _a10.5152/iao.2019.5401
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKüçük Kurtulgan, Hande
245 0 0 _aThe Analysis of GJB2, GJB3, and GJB6 Gene Mutations in Patients with Hereditary Non-Syndromic Hearing Loss Living in Sivas.
_h[electronic resource]
260 _bThe journal of international advanced otology
_cDec 2019
300 _a373-378 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aAged
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aConnexin 26
650 0 4 _aConnexin 30
_xgenetics
650 0 4 _aConnexins
_xgenetics
650 0 4 _aConsanguinity
650 0 4 _aFemale
650 0 4 _aGene Frequency
650 0 4 _aGenotype
650 0 4 _aHearing Loss, Sensorineural
_xgenetics
650 0 4 _aHeterozygote
650 0 4 _aHomozygote
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMutation
650 0 4 _aTurkey
650 0 4 _aYoung Adult
700 1 _aAltuntaş, Emine Elif
700 1 _aYıldırım, Malik Ejder
700 1 _aÖzdemir, Öztürk
700 1 _aBağcı, Binnur
700 1 _aSezgin, İlhan
773 0 _tThe journal of international advanced otology
_gvol. 15
_gno. 3
_gp. 373-378
856 4 0 _uhttps://doi.org/10.5152/iao.2019.5401
_zAvailable from publisher's website
999 _c30430166
_d30430166