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

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

Publication at Faculty of Physical Education and Sport |

2002

Abstract

Homocystinuria, CBS, prenatal diagnosis

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