1x0v: Difference between revisions
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{{STRUCTURE_1x0v| PDB=1x0v | SCENE= }} | {{STRUCTURE_1x0v| PDB=1x0v | SCENE= }} | ||
===Crystal Structure of Homo Sapien Glycerol-3-Phosphate Dehydrogenase 1=== | ===Crystal Structure of Homo Sapien Glycerol-3-Phosphate Dehydrogenase 1=== | ||
{{ABSTRACT_PUBMED_16460752}} | |||
==Disease== | |||
[[http://www.uniprot.org/uniprot/GPDA_HUMAN GPDA_HUMAN]] Defects in GPD1 are a cause of hypertriglyceridemia, transient infantile (HTGTI) [MIM:[http://omim.org/entry/614480 614480]]. An autosomal recessive disorder characterized by onset of moderate to severe transient hypertriglyceridemia in infancy that normalizes with age. The hypertriglyceridemia is associated with hepatomegaly, moderately elevated transaminases, persistent fatty liver, and the development of hepatic fibrosis.<ref>PMID:22226083</ref> | |||
==About this Structure== | ==About this Structure== | ||
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==Reference== | ==Reference== | ||
<ref group="xtra">PMID:016460752</ref><references group="xtra"/> | <ref group="xtra">PMID:016460752</ref><references group="xtra"/><references/> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Ou, X.]] | [[Category: Ou, X.]] | ||
