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Pyridoxal phosphate dependency, a newly recognized treatable catastrophic epileptic encephalopathy.

Publication ,  Journal Article
Pearl, PL; Gospe, SM
Published in: J Inherit Metab Dis
February 2007

Duke Scholars

Published In

J Inherit Metab Dis

DOI

EISSN

1573-2665

Publication Date

February 2007

Volume

30

Issue

1

Start / End Page

2 / 4

Location

United States

Related Subject Headings

  • Pyridoxine
  • Pyridoxaminephosphate Oxidase
  • Pyridoxal Phosphate
  • Metabolism, Inborn Errors
  • Infant, Newborn
  • Humans
  • Genetics & Heredity
  • Epilepsy
  • Aldehyde Dehydrogenase
  • 3202 Clinical sciences
 

Citation

APA
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ICMJE
MLA
NLM
Pearl, P. L., & Gospe, S. M. (2007). Pyridoxal phosphate dependency, a newly recognized treatable catastrophic epileptic encephalopathy. J Inherit Metab Dis, 30(1), 2–4. https://doi.org/10.1007/s10545-008-9974-1
Pearl, P. L., and S. M. Gospe. “Pyridoxal phosphate dependency, a newly recognized treatable catastrophic epileptic encephalopathy.J Inherit Metab Dis 30, no. 1 (February 2007): 2–4. https://doi.org/10.1007/s10545-008-9974-1.
Pearl, P. L., and S. M. Gospe. “Pyridoxal phosphate dependency, a newly recognized treatable catastrophic epileptic encephalopathy.J Inherit Metab Dis, vol. 30, no. 1, Feb. 2007, pp. 2–4. Pubmed, doi:10.1007/s10545-008-9974-1.
Journal cover image

Published In

J Inherit Metab Dis

DOI

EISSN

1573-2665

Publication Date

February 2007

Volume

30

Issue

1

Start / End Page

2 / 4

Location

United States

Related Subject Headings

  • Pyridoxine
  • Pyridoxaminephosphate Oxidase
  • Pyridoxal Phosphate
  • Metabolism, Inborn Errors
  • Infant, Newborn
  • Humans
  • Genetics & Heredity
  • Epilepsy
  • Aldehyde Dehydrogenase
  • 3202 Clinical sciences