scholarly journals Familial Congenital Methemoglobinemia in Pomeranian Dogs Caused by a Missense Variant in the NADH-Cytochrome B5 Reductase Gene

2018 ◽  
Vol 32 (1) ◽  
pp. 165-171 ◽  
Author(s):  
H. Shino ◽  
Y. Otsuka-Yamasaki ◽  
T. Sato ◽  
K. Ooi ◽  
O. Inanami ◽  
...  
Keyword(s):  
Cytochrome B5 ◽  
Missense Variant ◽  
Cytochrome B5 Reductase ◽  
Reductase Gene ◽  
Nadh Cytochrome

The organization and the complete nucleotide sequence of the human NADH-cytochrome b5 reductase gene

Gene ◽  
1989 ◽  
Vol 80 (2) ◽  
pp. 353-361 ◽  
Author(s):  
Tomatsu Shunji ◽  
Kobayashi Yasushi ◽  
Fukumaki Yasuyuki ◽  
Yubisui Toshitsugu ◽  
Orii Tadao ◽  
...  
Keyword(s):  
Nucleotide Sequence ◽  
Complete Nucleotide Sequence ◽  
Cytochrome B5 ◽  
Cytochrome B5 Reductase ◽  
Reductase Gene ◽  
Nadh Cytochrome

A novel G143D mutation in the NADH-cytochrome b5 reductase gene in an Indian patient with type I recessive hereditary methemoglobinemia

2008 ◽  
Vol 40 (3) ◽  
pp. 323-327 ◽  
Author(s):  
Prabhakar S. Kedar ◽  
Prashant Warang ◽  
Anita H. Nadkarni ◽  
Roshan B. Colah ◽  
Kanjaksha Ghosh
Keyword(s):  
Cytochrome B5 ◽  
Type I ◽  
Indian Patient ◽  
Cytochrome B5 Reductase ◽  
Reductase Gene ◽  
Nadh Cytochrome

Compound heterozygosity of two missense mutations in the NADH-cytochrome b5 reductase gene of a Polish patient with type I recessive congenital methaemoglobinaemia

2003 ◽  
Vol 70 (6) ◽  
pp. 404-409 ◽  
Author(s):  
Dorota Grabowska ◽  
Danuta Plochocka ◽  
Ewa Jablonska-Skwiecinska ◽  
Anna Chelstowska ◽  
Irmina Lewandowska ◽  
...  
Keyword(s):  
Cytochrome B5 ◽  
Type I ◽  
Missense Mutations ◽  
Compound Heterozygosity ◽  
Cytochrome B5 Reductase ◽  
Reductase Gene ◽  
Nadh Cytochrome ◽  
Polish Patient

Recessive hereditary methemoglobinemia: Two novel mutations in the NADH-cytochrome b5 reductase gene

2008 ◽  
Vol 41 (1) ◽  
pp. 50-55 ◽  
Author(s):  
Elisa Fermo ◽  
Paola Bianchi ◽  
Cristina Vercellati ◽  
Anna Paola Marcello ◽  
Massimo Garatti ◽  
...  
Keyword(s):  
Cytochrome B5 ◽  
Novel Mutations ◽  
Cytochrome B5 Reductase ◽  
Reductase Gene ◽  
Nadh Cytochrome

scholarly journals Molecular basis of hereditary methaemoglobinaemia, types I and II: two novel mutations in the NADH-cytochrome b5 reductase gene

1998 ◽  
Vol 103 (4) ◽  
pp. 922-930 ◽  
Author(s):  
Koichiro Higasa ◽  
Jun-Ichi Manabe ◽  
Toshitsuga Yubisui ◽  
Hideki Sumimoto ◽  
Parichat Pung-amritt ◽  
...  
Keyword(s):  
Molecular Basis ◽  
Cytochrome B5 ◽  
Novel Mutations ◽  
Cytochrome B5 Reductase ◽  
Reductase Gene ◽  
Nadh Cytochrome
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