RT-PCR and direct sequence analyses were used to define mutations in the cystathionine b -synthase (CBS) gene in two unrelated male patients with vitamin B6 nonresponsive homocystinuria. Both patients were compound heterozygotes for CBS alleles containing point mutations. One patient had a maternall
Chromosomal mapping and mutational analysis of the coding region of the glycogen synthase kinase-3α and β isoforms in patients with NIDDM
✍ Scribed by L. Hansen; K. C. Arden; S. B. Rasmussen; C. S. Viars; H. Vestergaard; T. Hansen; A. M. Møller; J. R. Woodgett; O. Pedersen
- Publisher
- Springer
- Year
- 1997
- Tongue
- English
- Weight
- 337 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0012-186X
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