| 000 | 01528 a2200505 4500 | ||
|---|---|---|---|
| 005 | 20250515005152.0 | ||
| 264 | 0 | _c20060613 | |
| 008 | 200606s 0 0 eng d | ||
| 022 | _a1098-1004 | ||
| 024 | 7 |
_a10.1002/humu.9384 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aKalay, E | |
| 245 | 0 | 0 |
_aFour novel TMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing loss. _h[electronic resource] |
| 260 |
_bHuman mutation _cDec 2005 |
||
| 300 |
_a591 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 | _aAmino Acid Sequence |
| 650 | 0 | 4 | _aConnexin 26 |
| 650 | 0 | 4 |
_aConnexins _xgenetics |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aFrameshift Mutation |
| 650 | 0 | 4 | _aGenetic Linkage |
| 650 | 0 | 4 | _aGenetic Testing |
| 650 | 0 | 4 | _aHaplotypes |
| 650 | 0 | 4 |
_aHearing Loss _xcongenital |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMembrane Proteins _xchemistry |
| 650 | 0 | 4 | _aMolecular Sequence Data |
| 650 | 0 | 4 | _aMutation, Missense |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aSequence Alignment |
| 650 | 0 | 4 | _aTurkey |
| 700 | 1 | _aKaraguzel, A | |
| 700 | 1 | _aCaylan, R | |
| 700 | 1 | _aHeister, A | |
| 700 | 1 | _aCremers, F P M | |
| 700 | 1 | _aCremers, C W R J | |
| 700 | 1 | _aBrunner, H G | |
| 700 | 1 | _ade Brouwer, A P M | |
| 700 | 1 | _aKremer, H | |
| 773 | 0 |
_tHuman mutation _gvol. 26 _gno. 6 _gp. 591 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/humu.9384 _zAvailable from publisher's website |
| 999 |
_c15911452 _d15911452 |
||