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Published in 2020 at "Clinical Genetics"
DOI: 10.1111/cge.13843
Abstract: Pyridoxamine‐5′‐phosphate oxidase (PNPO) deficiency is an autosomal recessive pyridoxal 5′‐phosphate (PLP)‐vitamin‐responsive epileptic encephalopathy. The emerging feature of PNPO deficiency is the occurrence of refractory seizures in the first year of life. Pre‐maturity and fetal distress,…
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Keywords:
pyridoxamine phosphate;
oxidase deficiency;
deficiency;
phosphate oxidase ... See more keywords