Published in:

01-11-2002

CblE type of homocystinuria due to methionine synthase reductase deficiency: Clinical and molecular studies and prenatal diagnosis in two families

Authors: P. Zavaď'áková, B. Fowler, J. Zeman, T. Suormala, K. Pšistoupilová, V. Kožich

Published in: Journal of Inherited Metabolic Disease | Issue 6/2002