| 000 | 01291 a2200373 4500 | ||
|---|---|---|---|
| 005 | 20250513184829.0 | ||
| 264 | 0 | _c19990910 | |
| 008 | 199909s 0 0 eng d | ||
| 022 | _a0141-8955 | ||
| 024 | 7 |
_a10.1023/a:1005599903632 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aGärtner, J | |
| 245 | 0 | 0 |
_aMutations in PEX1 in peroxisome biogenesis disorders: G843D and a mild clinical phenotype. _h[electronic resource] |
| 260 |
_bJournal of inherited metabolic disease _cMay 1999 |
||
| 300 |
_a311-3 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aATPases Associated with Diverse Cellular Activities |
| 650 | 0 | 4 |
_aAspartic Acid _xgenetics |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 |
_aGlycine _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 |
_aMembrane Proteins _xgenetics |
| 650 | 0 | 4 | _aMicrobodies |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aPeroxisomal Disorders _xgenetics |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aZellweger Syndrome _xgenetics |
| 700 | 1 | _aPreuss, N | |
| 700 | 1 | _aBrosius, U | |
| 700 | 1 | _aBiermanns, M | |
| 773 | 0 |
_tJournal of inherited metabolic disease _gvol. 22 _gno. 3 _gp. 311-3 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1023/a:1005599903632 _zAvailable from publisher's website |
| 999 |
_c10342746 _d10342746 |
||