Higasa, K <br/><br/>
Molecular basis of hereditary methaemoglobinaemia, types I and II: two novel mutations in the NADH-cytochrome b5 reductase gene.  [electronic resource] 

 -  British journal of haematology  Dec 1998 
 - 922-30 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0007-1048 
<br/><br/><label>Standard No.: </label>10.1046/j.1365-2141.1998.01123.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Substitution<br/>Cytochrome Reductases--genetics<br/>Cytochrome-B(5) Reductase<br/>Female<br/>Hot Temperature<br/>Humans<br/>Male<br/>Methemoglobinemia--genetics<br/>Mutation, Missense--genetics<br/>Pedigree<br/>Point Mutation--genetics<br/>Sequence Analysis<br/>Spectrum Analysis