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A novel PHKA2 mutation in a Chinese child with glycogen storage disease type IXa: a case report and literature review

BACKGROUND: PHKA2 gene mutations can cause liver phosphorylase kinase (PhK) deficiency, resulting in glycogen storage disease type IXa (GSD IXa). Elevated liver transaminase levels and liver enlargement are the most frequent phenotypes of GSD IXa. However, whether the phenotypes are applicable to Ch...

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Detalhes bibliográficos
Publicado no:BMC Med Genet
Main Authors: Fu, Junling, Wang, Tong, Xiao, Xinhua
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2019
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6441210/
https://ncbi.nlm.nih.gov/pubmed/30925902
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-019-0789-8
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