Molecular basis of two novel mutations found in type I methemoglobinemia.
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Nitrate and periplasmic nitrate reductasesHuman cytochrome b5 reductase: structure, function, and potential applications.Genetic variation in CYB5R3 is associated with methemoglobin levels in preterm infants receiving nitric oxide therapy.A patient with both methemoglobinemia and G6PD deficiency: A therapeutic conundrum.Re‐evaluation of potassium nitrite (E 249) and sodium nitrite (E 250) as food additivesClinical spectrum and molecular basis of recessive congenital methemoglobinemia in India.
P2860
Molecular basis of two novel mutations found in type I methemoglobinemia.
description
2011 nî lūn-bûn
@nan
2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Molecular basis of two novel mutations found in type I methemoglobinemia.
@ast
Molecular basis of two novel mutations found in type I methemoglobinemia.
@en
Molecular basis of two novel mutations found in type I methemoglobinemia.
@nl
type
label
Molecular basis of two novel mutations found in type I methemoglobinemia.
@ast
Molecular basis of two novel mutations found in type I methemoglobinemia.
@en
Molecular basis of two novel mutations found in type I methemoglobinemia.
@nl
prefLabel
Molecular basis of two novel mutations found in type I methemoglobinemia.
@ast
Molecular basis of two novel mutations found in type I methemoglobinemia.
@en
Molecular basis of two novel mutations found in type I methemoglobinemia.
@nl
P2093
P2860
P1476
Molecular basis of two novel mutations found in type I methemoglobinemia
@en
P2093
Bindu Lingam
Felipe R Lorenzo
John D Phillips
Josef T Prchal
Roberto Nussenzveig
Stanley L Schrier
P2860
P304
P356
10.1016/J.BCMD.2011.01.005
P577
2011-02-24T00:00:00Z