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Mutation analysis of SLC37A4 in a patient with glycogen storage disease-type Ib

OBJECTIVE: The aim of the study was to investigate the relationship between SLC37A4 gene mutation and clinical phenotype in a patient with glycogen storage disease-type I. METHODS: The clinical data of one patient with glycogen storage disease-type I accumulation syndrome and the results of SLC37A4...

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Detalhes bibliográficos
Publicado no:J Int Med Res
Main Authors: Zhang, Yamei, Sun, Huihui, Wan, Naijun
Formato: Artigo
Idioma:Inglês
Publicado em: SAGE Publications 2019
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7045669/
https://ncbi.nlm.nih.gov/pubmed/31617422
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0300060519867819
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