Found: 4
Select item for more details and to access through your institution.
Apolipoprotein E polymorphism and serum concentrations in patients with glycogen storage disease type Ia.
- Published in:
- Journal of Inherited Metabolic Disease, 2000, v. 23, n. 2, p. 107, doi. 10.1023/A:1005605513534
- By:
- Publication type:
- Article
Crigler–Najjar type II syndrome may result from several types and combinations of mutations in the UGT1A1 gene.
- Published in:
- 2006
- By:
- Publication type:
- Letter
Allelic heterogeneity of Crigler–Najjar type I syndrome: a study of 24 cases.
- Published in:
- 2004
- By:
- Publication type:
- Letter
Allelic heterogeneity of glycogen storage disease type Ib in French patients: A study of 11 cases.
- Published in:
- Journal of Inherited Metabolic Disease, 2004, v. 27, n. 5, p. 621, doi. 10.1023/B:BOLI.0000042987.43395.c6
- By:
- Publication type:
- Article