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Study of paediatric patients with the clinical and biochemical phenotype of glucose transporter type 1 deficiency syndrome
Estudio de pacientes pediátricos con fenotipo clínico y bioquímico de síndrome de déficit de transportador de glucosa cerebral (GLUT-1)
M. Jiménez Legidoa,
Corresponding author
maria_jimenez_11@hotmail.com

Corresponding author.
, C. Cortés Ledesmaa, B. Bernardino Cuestaa, L. López Marína,d, V. Cantarín Extremeraa,d, C. Pérez-Cerdáb, B. Pérez Gonzálezb, E. López Martínc, L. González Gutiérrez-Solanaa,d
a Sección de Neuropediatría, Hospital Infantil Universitario Niño Jesús, Madrid, Spain
b Centro de Diagnóstico de Enfermedades Moleculares (CEDEM), Madrid, Spain
c Instituto de Investigación de Enfermedades Raras (IIER) & Centro de Investigación Biomédica en Red para Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Madrid, Spain
d Grupo Clínico Vinculado a CIBERER (GCV6)
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ISSN: 21735808
Original language: English
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