The authors wish to correct a mistake which occurred in the reporting of one of the mutations. The mutation reported as 683insT is actually an insertion G mutation, and should thus be called 683insG.
Identification of P gene mutations in individuals with oculocutaneous albinism in sub-Saharan Africa
β Scribed by Robyn Kerr; Gwynneth Stevens; Prashiela Manga; Sarah Salm; Premila John; Tabitha Haw; Michele Ramsay
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 206 KB
- Volume
- 15
- Category
- Article
- ISSN
- 1059-7794
No coin nor oath required. For personal study only.
β¦ Synopsis
Communicated by
π SIMILAR VOLUMES
Even though, other health risks of mobile phone use are still under debate, the results with regard to motor vehicle accidents are unequivocal. The use of cellular telephones is associated with a reduced driving performance and a higher risk of a collision during the brief period of a call. The aim
## Communicated by JΓΌrgen Horst Mucopolysaccharidosis type IIIA (MPS IIIA or Sanfilippo A disease) is a storage disorder caused by deficiency of the lysosomal enzyme sulfamidase. Mutation screening, using SSCP/heteroduplex analyses on cDNA and genomic DNA fragments, was performed in a group of 42