| 000 | 01624 a2200469 4500 | ||
|---|---|---|---|
| 005 | 20250513141650.0 | ||
| 264 | 0 | _c19980604 | |
| 008 | 199806s 0 0 eng d | ||
| 022 | _a1059-7794 | ||
| 024 | 7 |
_a10.1002/(SICI)1098-1004(1998)11:4<275::AID-HUMU4>3.0.CO;2-L _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aKim, E K | |
| 245 | 0 | 0 |
_aIdentification of three novel mutations and a high frequency of the Arg778Leu mutation in Korean patients with Wilson disease. _h[electronic resource] |
| 260 |
_bHuman mutation _c1998 |
||
| 300 |
_a275-8 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aAdenosine Triphosphatases _xgenetics |
| 650 | 0 | 4 | _aAlleles |
| 650 | 0 | 4 | _aBase Sequence |
| 650 | 0 | 4 |
_aCarrier Proteins _xgenetics |
| 650 | 0 | 4 | _aCase-Control Studies |
| 650 | 0 | 4 | _aCation Transport Proteins |
| 650 | 0 | 4 | _aCopper-Transporting ATPases |
| 650 | 0 | 4 |
_aDNA Primers _xgenetics |
| 650 | 0 | 4 | _aGene Frequency |
| 650 | 0 | 4 |
_aHepatolenticular Degeneration _xenzymology |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aKorea |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aPoint Mutation |
| 650 | 0 | 4 | _aPolymerase Chain Reaction |
| 650 | 0 | 4 | _aPolymorphism, Single-Stranded Conformational |
| 650 | 0 | 4 | _aSequence Deletion |
| 700 | 1 | _aYoo, O J | |
| 700 | 1 | _aSong, K Y | |
| 700 | 1 | _aYoo, H W | |
| 700 | 1 | _aChoi, S Y | |
| 700 | 1 | _aCho, S W | |
| 700 | 1 | _aHahn, S H | |
| 773 | 0 |
_tHuman mutation _gvol. 11 _gno. 4 _gp. 275-8 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/(SICI)1098-1004(1998)11:4<275::AID-HUMU4>3.0.CO;2-L _zAvailable from publisher's website |
| 999 |
_c9521935 _d9521935 |
||