| 000 | 01735 a2200541 4500 | ||
|---|---|---|---|
| 005 | 20250513121642.0 | ||
| 264 | 0 | _c19970710 | |
| 008 | 199707s 0 0 eng d | ||
| 022 | _a0002-9297 | ||
| 024 | 7 |
_a10.1086/515459 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aNanji, M S | |
| 245 | 0 | 0 |
_aHaplotype and mutation analysis in Japanese patients with Wilson disease. _h[electronic resource] |
| 260 |
_bAmerican journal of human genetics _cJun 1997 |
||
| 300 |
_a1423-9 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aAdenosine Triphosphatases _xgenetics |
| 650 | 0 | 4 | _aBase Sequence |
| 650 | 0 | 4 |
_aCarrier Proteins _xgenetics |
| 650 | 0 | 4 | _aCation Transport Proteins |
| 650 | 0 | 4 | _aCopper-Transporting ATPases |
| 650 | 0 | 4 |
_aDNA _xblood |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 | _aDNA Primers |
| 650 | 0 | 4 | _aDNA Transposable Elements |
| 650 | 0 | 4 | _aExons |
| 650 | 0 | 4 | _aGenetic Markers |
| 650 | 0 | 4 | _aHaplotypes |
| 650 | 0 | 4 |
_aHepatolenticular Degeneration _xblood |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aJapan |
| 650 | 0 | 4 | _aMolecular Sequence Data |
| 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 | _aRepetitive Sequences, Nucleic Acid |
| 650 | 0 | 4 | _aSequence Deletion |
| 700 | 1 | _aNguyen, V T | |
| 700 | 1 | _aKawasoe, J H | |
| 700 | 1 | _aInui, K | |
| 700 | 1 | _aEndo, F | |
| 700 | 1 | _aNakajima, T | |
| 700 | 1 | _aAnezaki, T | |
| 700 | 1 | _aCox, D W | |
| 773 | 0 |
_tAmerican journal of human genetics _gvol. 60 _gno. 6 _gp. 1423-9 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1086/515459 _zAvailable from publisher's website |
| 999 |
_c9180079 _d9180079 |
||