| 000 | 01690 a2200517 4500 | ||
|---|---|---|---|
| 005 | 20250514031805.0 | ||
| 264 | 0 | _c20021025 | |
| 008 | 200210s 0 0 eng d | ||
| 022 | _a0031-3998 | ||
| 024 | 7 |
_a10.1203/00006450-200205000-00009 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aReich, Susanne | |
| 245 | 0 | 0 |
_aAn unexpectedly high frequency of hypergalactosemia in an immigrant Bosnian population revealed by newborn screening. _h[electronic resource] |
| 260 |
_bPediatric research _cMay 2002 |
||
| 300 |
_a598-601 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 |
_aAdenosine Triphosphate _xmetabolism |
| 650 | 0 | 4 | _aAmino Acid Sequence |
| 650 | 0 | 4 | _aAmino Acid Substitution |
| 650 | 0 | 4 |
_aBerlin _xepidemiology |
| 650 | 0 | 4 | _aBinding Sites |
| 650 | 0 | 4 |
_aBosnia and Herzegovina _xethnology |
| 650 | 0 | 4 |
_aCataract _xetiology |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aGalactokinase _xchemistry |
| 650 | 0 | 4 |
_aGalactosemias _xcomplications |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aIncidence |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMolecular Sequence Data |
| 650 | 0 | 4 | _aMutation, Missense |
| 650 | 0 | 4 | _aNeonatal Screening |
| 650 | 0 | 4 | _aPoint Mutation |
| 650 | 0 | 4 |
_aTurkey _xethnology |
| 700 | 1 | _aHennermann, Julia | |
| 700 | 1 | _aVetter, Barbara | |
| 700 | 1 | _aNeumann, Luitgard M | |
| 700 | 1 | _aShin, Yoon S | |
| 700 | 1 | _aSöling, Ariane | |
| 700 | 1 | _aMönch, Eberhard | |
| 700 | 1 | _aKulozik, Andreas E | |
| 773 | 0 |
_tPediatric research _gvol. 51 _gno. 5 _gp. 598-601 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1203/00006450-200205000-00009 _zAvailable from publisher's website |
| 999 |
_c11879381 _d11879381 |
||