000 01429 a2200421 4500
005 20250515152207.0
264 0 _c20090821
008 200908s 0 0 eng d
022 _a1808-8694
024 7 _a10.1016/S1808-8694(15)31392-6
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aPupo, Altair Cadrobbi
245 0 0 _aStudy of a Brazilian family presenting non-syndromic hearing loss with mitochondrial inheritance.
_h[electronic resource]
260 _bBrazilian journal of otorhinolaryngology
_c
300 _a786-789 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdult
650 0 4 _aAudiometry
650 0 4 _aBrazil
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aDNA, Mitochondrial
_xgenetics
650 0 4 _aGenes, Mitochondrial
_xgenetics
650 0 4 _aGenetic Predisposition to Disease
650 0 4 _aHearing Loss
_xgenetics
650 0 4 _aHearing Loss, Sensorineural
_xgenetics
650 0 4 _aHumans
650 0 4 _aMiddle Aged
650 0 4 _aMutation
650 0 4 _aPedigree
700 1 _aPirana, Sulene
700 1 _aSpinelli, Mauro
700 1 _aLezirovitz, Karina
700 1 _aNetto, Regina C Mingroni
700 1 _aMacedo, Lisandra S
773 0 _tBrazilian journal of otorhinolaryngology
_gvol. 74
_gno. 5
_gp. 786-789
856 4 0 _uhttps://doi.org/10.1016/S1808-8694(15)31392-6
_zAvailable from publisher's website
999 _c18534479
_d18534479