Achondrogenesis type 1B (ACG-lB), atelosteogenesis type 2 (A0-2), and diastrophic dysplasia (DTD) are recessively inherited chondrodysplasias of decreasing severity caused by mutations in the diastrophic dysplasia sul- fate transporter (DTDST) gene on chromosome 5. In these conditions, sulfate trans
✦ LIBER ✦
Sulfate Transport in Chondrodysplasia,
✍ Scribed by Johanna HÄStbacka; Andrea Superti-Furga; William R. Wilcox; David L. Rimoin; Daniel H. Cohn; Eric S. Lander
- Book ID
- 119873775
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 332 KB
- Volume
- 785
- Category
- Article
- ISSN
- 0890-6564
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