Dihydrofolate Reductase Deficiency Due to a Homozygous DHFR Mutation Causes Megaloblastic Anemia and Cerebral Folate Deficiency Leading to Severe Neurologic Disease-Reference-Cited by-同舟云学术

Dihydrofolate Reductase Deficiency Due to a Homozygous DHFR Mutation Causes Megaloblastic Anemia and Cerebral Folate Deficiency Leading to Severe Neurologic Disease

Published:2011-02 Issue:2 Volume:88 Page:226-231
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Cario Holger,Smith Desirée E.C.,Blom Henk,Blau Nenad,Bode Harald,Holzmann Karlheinz,Pannicke Ulrich,Hopfner Karl-Peter,Rump Eva-Maria,Ayric Zuleya,Kohne Elisabeth,Debatin Klaus-Michael,Smulders Yvo,Schwarz Klaus

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference18 articles.

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2. Acquired and inherited disorders of cobalamin and folate in children;Whitehead;Br. J. Haematol.,2006

3. Dihydrofolate reductase deficiency causing megaloblastic anemia in two families;Tauro;N. Engl. J. Med.,1976

4. Congenital megaloblastic anemia responsive to N5-formyl tetrafolic acid administration;Walters;J. Pediatr.,1967

5. Inborn errors of folate metabolism (second of two parts);Erbe;N. Engl. J. Med.,1975

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