Genetic defects of thiamine transport and metabolism: A review of clinical phenotypes, genetics, and functional studies-Reference-Cited by-同舟云学术

Genetic defects of thiamine transport and metabolism: A review of clinical phenotypes, genetics, and functional studies

Author:

Marcé‐Grau Anna¹^ORCID,Martí‐Sánchez Laura²³,Baide‐Mairena Heidy¹,Ortigoza‐Escobar Juan D.⁴^ORCID,Pérez‐Dueñas Belén¹⁵^ORCID

Affiliation:

1. Pediatric Neurology Research Group Hospital Vall d'Hebron and Research Institute (VHIR) Barcelona Spain

2. Department of Clinical Biochemistry Hospital Sant Joan de Déu Barcelona Barcelona Spain

3. Universitat de Barcelona Barcelona Spain

4. Department of Child Neurology Hospital Sant Joan de Déu Barcelona Barcelona Spain

5. Centre for Biochemical Research in Rare Diseases (CIBERER) Valencia Spain

Funder

Fundació la Marató de TV3

Instituto de Salud Carlos III

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

Reference115 articles.

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