000 01366 a2200397 4500
005 20250517000727.0
264 0 _c20150624
008 201506s 0 0 eng d
022 _a1791-3004
024 7 _a10.3892/mmr.2014.2725
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aLi, Tung-Cheng
245 0 0 _aAssociation between mutations in the gap junction β4 gene and nonsyndromic hearing loss: genotype-phenotype correlation patterns.
_h[electronic resource]
260 _bMolecular medicine reports
_cJan 2015
300 _a619-24 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdolescent
650 0 4 _aChild
650 0 4 _aConnexins
_xchemistry
650 0 4 _aDeafness
_xdiagnosis
650 0 4 _aEar, Inner
_xdiagnostic imaging
650 0 4 _aGenetic Association Studies
650 0 4 _aGenotype
650 0 4 _aHearing Tests
650 0 4 _aHumans
650 0 4 _aMutation
650 0 4 _aPhenotype
650 0 4 _aSeverity of Illness Index
650 0 4 _aTemporal Bone
_xdiagnostic imaging
650 0 4 _aTomography, X-Ray Computed
700 1 _aWang, Wen-Hung
700 1 _aLi, Chuan
700 1 _aYang, Jiann-Jou
773 0 _tMolecular medicine reports
_gvol. 11
_gno. 1
_gp. 619-24
856 4 0 _uhttps://doi.org/10.3892/mmr.2014.2725
_zAvailable from publisher's website
999 _c24295767
_d24295767