| 000 | 01177 a2200349 4500 | ||
|---|---|---|---|
| 005 | 20250513230942.0 | ||
| 264 | 0 | _c20010405 | |
| 008 | 200104s 0 0 eng d | ||
| 022 | _a1018-4813 | ||
| 024 | 7 |
_a10.1038/sj.ejhg.5200569 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aLópez-Bigas, N | |
| 245 | 0 | 0 |
_aR32W variant in Connexin 31: mutation or polymorphism for deafness and skin disease? _h[electronic resource] |
| 260 |
_bEuropean journal of human genetics : EJHG _cJan 2001 |
||
| 300 |
_a70 p. _bdigital |
||
| 500 | _aPublication Type: Comment; Letter; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAmino Acid Substitution |
| 650 | 0 | 4 |
_aConnexins _xgenetics |
| 650 | 0 | 4 |
_aDeafness _xgenetics |
| 650 | 0 | 4 | _aFamily Health |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aPolymorphism, Genetic |
| 650 | 0 | 4 |
_aSkin Diseases _xgenetics |
| 700 | 1 | _aRabionet, R | |
| 700 | 1 | _aArbonés, M L | |
| 700 | 1 | _aEstivill, X | |
| 773 | 0 |
_tEuropean journal of human genetics : EJHG _gvol. 9 _gno. 1 _gp. 70 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1038/sj.ejhg.5200569 _zAvailable from publisher's website |
| 999 |
_c11114030 _d11114030 |
||