000 01402 a2200385 4500
005 20250515094618.0
264 0 _c20080229
008 200802s 0 0 eng d
022 _a1399-0004
024 7 _a10.1111/j.1399-0004.2007.00925.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aLabay, V
245 0 0 _aHaplogroup analysis supports a pathogenic role for the 7510T>C mutation of mitochondrial tRNA(Ser(UCN)) in sensorineural hearing loss.
_h[electronic resource]
260 _bClinical genetics
_cJan 2008
300 _a50-4 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't
650 0 4 _aDNA, Mitochondrial
_xgenetics
650 0 4 _aFamily Health
650 0 4 _aGenome, Mitochondrial
650 0 4 _aHaplotypes
650 0 4 _aHearing Loss, Sensorineural
_xgenetics
650 0 4 _aNorth America
650 0 4 _aPedigree
650 0 4 _aPoint Mutation
650 0 4 _aRNA, Transfer, Ser
_xgenetics
700 1 _aGarrido, G
700 1 _aMadeo, A C
700 1 _aNance, W E
700 1 _aFriedman, T B
700 1 _aFriedman, P L
700 1 _aDel Castillo, I
700 1 _aGriffith, A J
773 0 _tClinical genetics
_gvol. 73
_gno. 1
_gp. 50-4
856 4 0 _uhttps://doi.org/10.1111/j.1399-0004.2007.00925.x
_zAvailable from publisher's website
999 _c17544455
_d17544455