| 000 | 01376 a2200385 4500 | ||
|---|---|---|---|
| 005 | 20250513224708.0 | ||
| 264 | 0 | _c20010111 | |
| 008 | 200101s 0 0 eng d | ||
| 022 | _a1098-1004 | ||
| 024 | 7 |
_a10.1002/1098-1004(200012)16:6<502::AID-HUMU7>3.0.CO;2-4 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aPrasad, S | |
| 245 | 0 | 0 |
_aGenetic testing for hereditary hearing loss: connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA). _h[electronic resource] |
| 260 |
_bHuman mutation _cDec 2000 |
||
| 300 |
_a502-8 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 | _aAlleles |
| 650 | 0 | 4 |
_aAmino Acid Substitution _xgenetics |
| 650 | 0 | 4 |
_aArginine _xgenetics |
| 650 | 0 | 4 | _aConnexin 26 |
| 650 | 0 | 4 |
_aConnexins _xblood |
| 650 | 0 | 4 |
_aCysteine _xgenetics |
| 650 | 0 | 4 |
_aDeafness _xcongenital |
| 650 | 0 | 4 |
_aGenetic Testing _xmethods |
| 650 | 0 | 4 | _aGenetic Variation |
| 650 | 0 | 4 |
_aHearing Loss, Sensorineural _xcongenital |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aMutation _xgenetics |
| 650 | 0 | 4 |
_aSequence Deletion _xgenetics |
| 700 | 1 | _aCucci, R A | |
| 700 | 1 | _aGreen, G E | |
| 700 | 1 | _aSmith, R J | |
| 773 | 0 |
_tHuman mutation _gvol. 16 _gno. 6 _gp. 502-8 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/1098-1004(200012)16:6<502::AID-HUMU7>3.0.CO;2-4 _zAvailable from publisher's website |
| 999 |
_c11044345 _d11044345 |
||