| 000 | 01751 a2200517 4500 | ||
|---|---|---|---|
| 005 | 20250515093015.0 | ||
| 264 | 0 | _c20080416 | |
| 008 | 200804s 0 0 eng d | ||
| 022 | _a0742-3071 | ||
| 024 | 7 |
_a10.1111/j.1464-5491.2007.02285.x _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aWabitsch, M | |
| 245 | 0 | 0 |
_aHeterogeneity in disease severity in a family with a novel G68V GCK activating mutation causing persistent hyperinsulinaemic hypoglycaemia of infancy. _h[electronic resource] |
| 260 |
_bDiabetic medicine : a journal of the British Diabetic Association _cDec 2007 |
||
| 300 |
_a1393-9 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 |
_aBlood Glucose _xanalysis |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 |
_aCongenital Hyperinsulinism _xgenetics |
| 650 | 0 | 4 | _aFamily Health |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aGlucokinase _xgenetics |
| 650 | 0 | 4 | _aGlucose Tolerance Test |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aIslets of Langerhans _xenzymology |
| 650 | 0 | 4 |
_aKATP Channels _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 | _aMutation, Missense |
| 650 | 0 | 4 | _aPedigree |
| 700 | 1 | _aLahr, G | |
| 700 | 1 | _aVan de Bunt, M | |
| 700 | 1 | _aMarchant, C | |
| 700 | 1 | _aLindner, M | |
| 700 | 1 | _avon Puttkamer, J | |
| 700 | 1 | _aFenneberg, A | |
| 700 | 1 | _aDebatin, K M | |
| 700 | 1 | _aKlein, R | |
| 700 | 1 | _aEllard, S | |
| 700 | 1 | _aClark, A | |
| 700 | 1 | _aGloyn, A L | |
| 773 | 0 |
_tDiabetic medicine : a journal of the British Diabetic Association _gvol. 24 _gno. 12 _gp. 1393-9 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1111/j.1464-5491.2007.02285.x _zAvailable from publisher's website |
| 999 |
_c17494520 _d17494520 |
||