✦ LIBER ✦
Loss of matrilin 1 does not exacerbate the skeletal phenotype in a mouse model of multiple epiphyseal dysplasia caused by a Matn3 V194D mutation
✍ Scribed by Peter A. Bell; Katarzyna A. Piróg; Maryline Fresquet; David J. Thornton; Raymond P. Boot-Handford; Michael D. Briggs
- Book ID
- 112002605
- Publisher
- John Wiley and Sons
- Year
- 2012
- Tongue
- English
- Weight
- 342 KB
- Volume
- 64
- Category
- Article
- ISSN
- 0004-3591
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