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Journal of Neurology, Neurosurgery, and Psychiatry logoLink to Journal of Neurology, Neurosurgery, and Psychiatry
. 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

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Selected References

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

  1. 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]
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