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Article

Inherent lipid metabolic dysfunction in glycogen storage disease IIIa.

Biochemical and biophysical research communications - 5 Dec 2014

Li Xin-Hua, Gong Qi-Ming, Ling Yun, Huang Chong, Yu De-Min, Gu Lei-Lei, Liao Xiang-Wei, Zhang Dong-Hua, Hu Xi-Qi, Han Yue, Kong Xiao-Fei, Zhang Xin-Xin

Abstract excerpt

We studied two patients from a nonconsanguineous family with life-long abnormal liver function, hepatomegaly and abnormal fatty acid profiles. Abnormal liver function, hypoglycemia and muscle weakness are observed in various genetic diseases, including medium-chain acyl-CoA dehydrogenase (MCAD) d...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 25451272
DOI: 10.1016/j.bbrc.2014.10.096

Genes

AGL
ACADL
ACADM

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-25451272-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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