| 000 | 01525 a2200409 4500 | ||
|---|---|---|---|
| 005 | 20250515164500.0 | ||
| 264 | 0 | _c20090602 | |
| 008 | 200906s 0 0 eng d | ||
| 022 | _a1545-5017 | ||
| 024 | 7 |
_a10.1002/pbc.22011 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aTitapiwatanakun, Ruetima | |
| 245 | 0 | 0 |
_aNovel splice site mutations in the gamma glutamyl carboxylase gene in a child with congenital combined deficiency of the vitamin K-dependent coagulation factors (VKCFD). _h[electronic resource] |
| 260 |
_bPediatric blood & cancer _cJul 2009 |
||
| 300 |
_a92-5 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_aBlood Coagulation Factors _xgenetics |
| 650 | 0 | 4 |
_aCarbon-Carbon Ligases _xdeficiency |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 |
_aCoagulation Protein Disorders _xcongenital |
| 650 | 0 | 4 | _aDiagnosis, Differential |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMixed Function Oxygenases _xgenetics |
| 650 | 0 | 4 |
_aMunchausen Syndrome _xdiagnosis |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
| 650 | 0 | 4 |
_aVitamin K _xadministration & dosage |
| 650 | 0 | 4 |
_aVitamin K Deficiency _xcongenital |
| 650 | 0 | 4 | _aVitamin K Epoxide Reductases |
| 700 | 1 | _aRodriguez, Vilmarie | |
| 700 | 1 | _aMiddha, Sumit | |
| 700 | 1 | _aDukek, Brian A | |
| 700 | 1 | _aPruthi, Rajiv K | |
| 773 | 0 |
_tPediatric blood & cancer _gvol. 53 _gno. 1 _gp. 92-5 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/pbc.22011 _zAvailable from publisher's website |
| 999 |
_c18776371 _d18776371 |
||