Genotypic and clinical analysis of 49 Chinese children with hepatic glycogen storage diseases

BACKGROUND: Glycogen storage disease (GSD) is a relatively rare inborn metabolic disorder, our study aims to investigate the genotypic and clinical feature of hepatic GSDs in China. METHODS: The clinical and genotypic data of 49 patients with hepatic GSDs were collected retrospectively and analyzed....

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Detalles Bibliográficos
Autores principales: Liang, Yan, Du, Caiqi, Wei, Hong, Zhang, Cai, Zhang, Min, Hu, Minghui, Fang, Feng, Luo, Xiaoping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7549605/
https://www.ncbi.nlm.nih.gov/pubmed/32772503
http://dx.doi.org/10.1002/mgg3.1444

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7549605/
https://www.ncbi.nlm.nih.gov/pubmed/32772503
http://dx.doi.org/10.1002/mgg3.1444

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