The molecular basis of leukocyte recruitment and its deficiencies
β Scribed by Schmidt, Sarah; Moser, Markus; Sperandio, Markus
- Book ID
- 120937877
- Publisher
- Elsevier Science
- Year
- 2013
- Tongue
- English
- Weight
- 820 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0161-5890
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The authors of this article have learned that the cDNA sequence numbering of the three novel mutations reported in the FTCD gene was incorrect. The authors regret this error but note that the mutations were reported correctly at the protein/amino acid level. The DNA mutations should have been repor
Glutamate formiminotransferase deficiency, an autosomal recessive disorder and the second most common inborn error of folate metabolism, is presumed to be due to defects in the bifunctional enzyme glutamate formiminotransferase-cyclodeaminase (FTCD). Features of a severe phenotype, first identified