Skip to main content

. 1996 Jan;60(1):107–108. doi: 10.1136/jnnp.60.1.107

Hereditary defect of cobalamin metabolism (homocystinuria and methylmalonic aciduria) of juvenile onset.

R Gold, U Bogdahn, L Kappos, K V Toyka, E R Baumgartner, B Fowler, U Wendel

PMCID: PMC486204 PMID: 8558138

107

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

Carmel R., Watkins D., Goodman S. I., Rosenblatt D. S. Hereditary defect of cobalamin metabolism (cblG mutation) presenting as a neurologic disorder in adulthood. N Engl J Med. 1988 Jun 30;318(26):1738–1741. doi: 10.1056/NEJM198806303182607. [DOI] [PubMed] [Google Scholar]
Shinnar S., Singer H. S. Cobalamin C mutation (methylmalonic aciduria and homocystinuria) in adolescence. A treatable cause of dementia and myelopathy. N Engl J Med. 1984 Aug 16;311(7):451–454. doi: 10.1056/NEJM198408163110707. [DOI] [PubMed] [Google Scholar]

ACTIONS

RESOURCES