Associated Papers
Molecular and Clinical Characterization of a Founder Mutation Causing G6PC3 Deficiency.
Zhen X et al.
Journal of Clinical Immunology, 2024
Molecular and clinical characterization of a founder mutation causing G6PC3 deficiency.
Zhen X et al.
Research Square, 2024
Molecular and clinical characterization of a founder mutation causing G6PC3 deficiency.
Zhen X et al.
Medrxiv : the Preprint Server for Health Sciences, 2024
Severe Congenital Neutropenia Type 4: A Rare Disease Harboring a G6pc3 Gene Pathogenic Variant Particular to the Mexican Population.
López-Rodríguez L et al.
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion, 2022
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