The most common mutation causing medium-chain acyl-CoA dehydrogenase deficiency is strongly associated with a particular haplotype in the region of the gene
Steen Kølvraa, Niels Gregersen, Alexandra I. F. Blakemore, Anne K. Schneidermann, Vibeke Winter, Brage S. Andresen, Diana Curtis, Paul C. Engel, Divry Pricille, William Rhead, Lars BolundVolume:
87
Language:
english
Pages:
4
DOI:
10.1007/bf00197161
Date:
August, 1991
File:
PDF, 395 KB
english, 1991