| 000 | 01037 a2200301 4500 | ||
|---|---|---|---|
| 005 | 20250516085005.0 | ||
| 264 | 0 | _c20121026 | |
| 008 | 201210s 0 0 eng d | ||
| 022 | _a1750-1172 | ||
| 024 | 7 |
_a10.1186/1750-1172-7-19 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aEggermann, Thomas | |
| 245 | 0 | 0 |
_aCystinuria: an inborn cause of urolithiasis. _h[electronic resource] |
| 260 |
_bOrphanet journal of rare diseases _cApr 2012 |
||
| 300 |
_a19 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Review | ||
| 650 | 0 | 4 |
_aAmino Acid Transport Systems, Basic _xgenetics |
| 650 | 0 | 4 |
_aAmino Acid Transport Systems, Neutral _xgenetics |
| 650 | 0 | 4 |
_aCystinuria _xgenetics |
| 650 | 0 | 4 | _aGenetic Testing |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aUrolithiasis _xetiology |
| 700 | 1 | _aVenghaus, Andreas | |
| 700 | 1 | _aZerres, Klaus | |
| 773 | 0 |
_tOrphanet journal of rare diseases _gvol. 7 _gp. 19 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1186/1750-1172-7-19 _zAvailable from publisher's website |
| 999 |
_c21682353 _d21682353 |
||