000 01774 a2200541 4500
005 20250516073127.0
264 0 _c20120709
008 201207s 0 0 eng d
022 _a1098-1004
024 7 _a10.1002/humu.22023
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aGutiérrez Cortés, Nicolás
245 0 0 _aNovel mitochondrial DNA mutations responsible for maternally inherited nonsyndromic hearing loss.
_h[electronic resource]
260 _bHuman mutation
_cApr 2012
300 _a681-9 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAminoglycosides
_xadverse effects
650 0 4 _aCell Line
650 0 4 _aCell Respiration
_xgenetics
650 0 4 _aCytochromes b
_xgenetics
650 0 4 _aDNA, Mitochondrial
650 0 4 _aFemale
650 0 4 _aHearing Loss
_xchemically induced
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMitochondria
_xgenetics
650 0 4 _aMothers
650 0 4 _aMutation
650 0 4 _aNADH Dehydrogenase
_xchemistry
650 0 4 _aPedigree
650 0 4 _aPhosphorylation
650 0 4 _aPolymorphism, Restriction Fragment Length
650 0 4 _aProtein Conformation
650 0 4 _aRNA, Transfer, Ile
_xgenetics
650 0 4 _aRNA, Transfer, Ser
_xgenetics
700 1 _aPertuiset, Claire
700 1 _aDumon, Elodie
700 1 _aBörlin, Marine
700 1 _aHebert-Chatelain, Etienne
700 1 _aPierron, Denis
700 1 _aFeldmann, Delphine
700 1 _aJonard, Laurence
700 1 _aMarlin, Sandrine
700 1 _aLetellier, Thierry
700 1 _aRocher, Christophe
773 0 _tHuman mutation
_gvol. 33
_gno. 4
_gp. 681-9
856 4 0 _uhttps://doi.org/10.1002/humu.22023
_zAvailable from publisher's website
999 _c21457817
_d21457817