𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Mutations in the MMAA Gene in Patients With the cblA Disorder of Vitamin B12 Metabolism

✍ Scribed by Jordan P. Lerner-Ellis; C. Melissa Dobson; Timothy Wai; David Watkins; Jamie C. Tirone; Daniel Leclerc; Carole Doré; Pierre Lepage; Roy A. Gravel; David S. Rosenblatt


Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
55 KB
Volume
25
Category
Article
ISSN
1059-7794

No coin nor oath required. For personal study only.

✦ Synopsis


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 ''Mutations in the MMAA Gene.'' The publisher regrets this error.

The mutation in exon 3 that was given as ''c440G.A(E147G)'' should have been ''c440G4A(G147E),'' as the amino acids were inverted. Additionally, two cell lines given in Table 3 were incorrectly listed. Cell line ''WG3038'' should be corrected to read ''WG3039,'' and ''WG3039'' should be corrected to read ''WG3038.'' Erratum received


📜 SIMILAR VOLUMES


Mutations in the MMAA gene in patients w
✍ Jordan P. Lerner-Ellis; C. Melissa Dobson; Timothy Wai; David Watkins; Jamie C. 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 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

Mutation analysis of the M6b gene in pat
✍ Narayanan, Vinodh; Olinsky, Shari; Dahle, Elizabeth; Naidu, Sakkubai; Zoghbi, Hu 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 22 KB 👁 2 views

Human Xp22.2 has been proposed as a candidate region for the Rett syndrome (RTT) gene. M6b, a member of the proteolipid protein gene family, was mapped to Xp22.2 within one of the RTT candidate regions. In this article we describe the structure of the M6b gene, refine the physical mapping of M6b bet