Compound heterozygosity of two missense mutations in the NADH-cytochrome b5 reductase gene of a Polish patient with type I recessive congenital methaemoglobinaemia.
about
Human cytochrome b5 reductase: structure, function, and potential applications.Molecular basis of two novel mutations found in type I methemoglobinemia.Recessive congenital methaemoglobinaemia: cytochrome b(5) reductase deficiency.Prenatal diagnosis of recessive congenital methaemoglobinaemia type II: novel mutation in the NADH-cytochrome b5 reductase gene leading to stop codon read-through.
P2860
Compound heterozygosity of two missense mutations in the NADH-cytochrome b5 reductase gene of a Polish patient with type I recessive congenital methaemoglobinaemia.
description
2003 nî lūn-bûn
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2003 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Compound heterozygosity of two ...... ongenital methaemoglobinaemia.
@ast
Compound heterozygosity of two ...... ongenital methaemoglobinaemia.
@en
type
label
Compound heterozygosity of two ...... ongenital methaemoglobinaemia.
@ast
Compound heterozygosity of two ...... ongenital methaemoglobinaemia.
@en
prefLabel
Compound heterozygosity of two ...... ongenital methaemoglobinaemia.
@ast
Compound heterozygosity of two ...... ongenital methaemoglobinaemia.
@en
P2093
P1476
Compound heterozygosity of two ...... ongenital methaemoglobinaemia.
@en
P2093
Danuta Plochocka
Dorota Grabowska
Ewa Jablonska-Skwiecinska
Irmina Lewandowska
Iwona Witos
Krystyna Staniszewska
Zofia Majewska
P304
P356
10.1034/J.1600-0609.2003.00070.X
P577
2003-06-01T00:00:00Z