क्यूआर कोड

Molybdenum cofactor biosynthesis in humans. Identification of two complementation groups of cofactor-deficient patients and preliminary characterization of a diffusible molybdopterin precursor.

Molybdenum cofactor deficiency is a devastating disease with affected patients displaying the symptoms of a combined deficiency of sulfite oxidase and xanthine dehydrogenase. Because of the extreme lability of the isolated, functional molybdenum cofactor, direct cofactor replacement therapy is not f...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:J Clin Invest
मुख्य लेखकों: Johnson, J L, Wuebbens, M M, Mandell, R, Shih, V E
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: American Society for Clinical Investigation 1989
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC303764/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2522104/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI113974
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