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Síndromes hereditarios del transporte de glucosa
Translated title of the contribution
:
Glucose transport hereditary diseases
Juan M. Pascual
Pediatrics
Physiology
Neurology & Neurotherapeutics - NE Neuro Pediatrics Section
Eugene Mcdermott Center For Human Growth & Development
Neurology & Neurotherapeutics
Research output
:
Contribution to journal
›
Review article
›
peer-review
6
Scopus citations
Overview
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Medicine & Life Sciences
Glut1 Deficiency Syndrome
100%
Inborn Genetic Diseases
77%
Glucose
52%
Mutation
46%
Glucose-Galactose Malabsorption
43%
Fanconi Syndrome
41%
Membranes
33%
Facilitative Glucose Transport Proteins
32%
Epilepsy
23%
Liver
14%
Brain
13%
Genes
11%