| 000 | 01519 a2200529 4500 | ||
|---|---|---|---|
| 005 | 20250517075206.0 | ||
| 264 | 0 | _c20170630 | |
| 008 | 201706s 0 0 eng d | ||
| 022 | _a1399-0004 | ||
| 024 | 7 |
_a10.1111/cge.12744 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aZhang, Q-J | |
| 245 | 0 | 0 |
_aHigh frequency of OTOF mutations in Chinese infants with congenital auditory neuropathy spectrum disorder. _h[electronic resource] |
| 260 |
_bClinical genetics _c09 2016 |
||
| 300 |
_a238-46 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAlleles |
| 650 | 0 | 4 | _aAudiometry |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aChina |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Predisposition to Disease |
| 650 | 0 | 4 |
_aHearing Disorders _xdiagnosis |
| 650 | 0 | 4 |
_aHearing Loss, Central _xdiagnosis |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMembrane Proteins _xgenetics |
| 650 | 0 | 4 | _aMutation |
| 700 | 1 | _aHan, B | |
| 700 | 1 | _aLan, L | |
| 700 | 1 | _aZong, L | |
| 700 | 1 | _aShi, W | |
| 700 | 1 | _aWang, H-Y | |
| 700 | 1 | _aXie, L-Y | |
| 700 | 1 | _aWang, H | |
| 700 | 1 | _aZhao, C | |
| 700 | 1 | _aZhang, C | |
| 700 | 1 | _aYin, Z-F | |
| 700 | 1 | _aWang, D-Y | |
| 700 | 1 | _aPetit, C | |
| 700 | 1 | _aGuan, J | |
| 700 | 1 | _aWang, Q-J | |
| 773 | 0 |
_tClinical genetics _gvol. 90 _gno. 3 _gp. 238-46 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1111/cge.12744 _zAvailable from publisher's website |
| 999 |
_c25676727 _d25676727 |
||