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High resolution melting analysis of the MMAA gene in patients with cblA and in those with undiagnosed methylmalonic aciduria

✍ Scribed by Laura Dempsey-Nunez; Margaret L. Illson; Jana Kent; Qiuying Huang; Alison Brebner; David Watkins; Brian M. Gilfix; Carl T. Wittwer; David S. Rosenblatt

Book ID
117999880
Publisher
Elsevier Science
Year
2012
Tongue
English
Weight
339 KB
Volume
107
Category
Article
ISSN
1096-7192

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πŸ“œ SIMILAR VOLUMES

Mutations in the MMAA gene in patients w
Mutations in the MMAA gene in patients with the cblA disorder of vitamin B12 metabolism
✍ Jordan P. Lerner-Ellis; C. Melissa Dobson; Timothy Wai; David Watkins; Jamie C. πŸ“‚ Article πŸ“… 2004 πŸ› John Wiley and Sons 🌐 English βš– 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
✍ Jordan P. Lerner-Ellis; C. Melissa Dobson; Timothy Wai; David Watkins; Jamie C. πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 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