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Inherited disorders of vitamin B12 metabolism

โœ Scribed by D.S. Rosenblatt; B.A. Cooper

Publisher
Elsevier Science
Year
1987
Tongue
English
Weight
714 KB
Volume
1
Category
Article
ISSN
0268-960X

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๐Ÿ“œ SIMILAR VOLUMES

Inherited disorders of vitamin B12 utili
Inherited disorders of vitamin B12 utilization
โœ David S. Rosenblatt; Bernard A. Cooper ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 495 KB

Inborn errors of vitamin B12 (cobalamin) metabolism are associated with homocystinuria and methylmalonic aciduria, either alone or in combination. A number of these disorders have provided the first evidence for the existence of important steps in the transport or metabolism of cobalamin in eukaryot

Mutations in the MMAA gene in patients w
Mutations in the MMAA gene in patients with the cblA disorder of vitamin B12 metabolism
โœ Jordan P. Lerner-Ellis; C. Melissa Dobson; Timothy Wai; David Watkins; Jamie C. ๐Ÿ“‚ Article ๐Ÿ“… 2004 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 160 KB

Mutations in the MMAA gene on human chromosome 4q31.21 result in vitamin B12-responsive methylmalonic aciduria (cblA complementation group) due to deficiency in the synthesis of adenosylcobalamin. Genomic DNA from 37 cblA patients, diagnosed on the basis of cellular adenosylcobalamin synthesis, meth

Mutations in the MMAA Gene in Patients W
Mutations in the MMAA Gene in Patients With the cblA Disorder of Vitamin B12 Metabolism
โœ Jordan P. Lerner-Ellis; C. Melissa Dobson; Timothy Wai; David Watkins; Jamie C. ๐Ÿ“‚ Article ๐Ÿ“… 2005 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 55 KB

The original article to which this Erratum refers was published in Human Mutation 24: 509-516 (2004). In the original article, the running header incorrectly read ''Mutations in the MMMA Gene,'' although it was corrected by the author during the proofing stage. The correct running header should read