Jenkins, M M <br/><br/>
A novel mutation found in the 3' domain of NADH-cytochrome B5 reductase in an African-American family with type I congenital methemoglobinemia.  [electronic resource] 

 -  Blood  Apr 1996 
 - 2993-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0006-4971 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Base Sequence<br/>Black People--genetics<br/>Cloning, Molecular<br/>Cytochrome Reductases--genetics<br/>Cytochrome-B(5) Reductase<br/>Female<br/>Humans<br/>Male<br/>Methemoglobinemia--congenital<br/>Molecular Sequence Data<br/>Pedigree<br/>Point Mutation<br/>Sequence Analysis<br/>Black or African American