Found: 12
Select item for more details and to access through your institution.
Correction to: Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme.
- Published in:
- 2021
- By:
- Publication type:
- Correction Notice
Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme.
- Published in:
- BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-021-01061-3
- By:
- Publication type:
- Article
Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme.
- Published in:
- BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-021-01061-3
- By:
- Publication type:
- Article
Novel splice site <italic>IDUA</italic> gene mutation in Tunisian pedigrees with hurler syndrome.
- Published in:
- Diagnostic Pathology, 2018, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13000-018-0710-3
- By:
- Publication type:
- Article
Molecular analysis in a GALNS study cohort of 15 Tunisian patients: description of a novel mutation.
- Published in:
- Diagnostic Pathology, 2016, v. 11, p. 1, doi. 10.1186/s13000-016-0498-y
- By:
- Publication type:
- Article
Identification of mutations that causes glucose-6-phosphate transporter defect in tunisian patients with glycogenosis type 1b.
- Published in:
- Diabetology & Metabolic Syndrome, 2023, v. 15, n. 1, p. 1, doi. 10.1186/s13098-023-01065-2
- By:
- Publication type:
- Article
Low erythrocyte catalase enzyme activity is correlated with high serum total homocysteine levels in tunisian patients with acute myocardial infarction.
- Published in:
- Diagnostic Pathology, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1746-1596-8-68
- By:
- Publication type:
- Article
Hsp70-2 gene polymorphism: susceptibility implication in Tunisian patients with coronary artery disease.
- Published in:
- Diagnostic Pathology, 2012, v. 7, n. 1, p. 88, doi. 10.1186/1746-1596-7-88
- By:
- Publication type:
- Article
Molecular analysis of iduronate -2- sulfatase gene in Tunisian patients with mucopolysaccharidosis type II.
- Published in:
- Diagnostic Pathology, 2011, v. 6, n. Suppl 1, p. 42, doi. 10.1186/1746-1596-6-42
- By:
- Publication type:
- Article
Molecular analysis of mucopolysaccharidosis type I in Tunisia: identification of novel mutation and eight Novel polymorphisms.
- Published in:
- Diagnostic Pathology, 2011, v. 6, n. Suppl 1, p. 39, doi. 10.1186/1746-1596-6-39
- By:
- Publication type:
- Article
Polymorphisms in Tunisian patients with N-acetylgalactosamine-6-sulfate sulfatase gene deficiency: Implication in Morquio A disease.
- Published in:
- Diagnostic Pathology, 2011, v. 6, n. 1, p. 11, doi. 10.1186/1746-1596-6-11
- By:
- Publication type:
- Article
Molecular characterization of CTNS mutations in Tunisian patients with ocular cystinosis.
- Published in:
- Diagnostic Pathology, 2022, v. 17, n. 1, p. 1, doi. 10.1186/s13000-022-01221-8
- By:
- Publication type:
- Article