✦ LIBER ✦
Recurrent heterozygous missense mutation, p.Gly573Ser, in the TRPV3 gene in an Indian boy with sporadic Olmsted syndrome
✍ Scribed by J.E. Lai-Cheong; G. Sethuraman; M. Ramam; K. Stone; M.A. Simpson; J.A. McGrath
- Book ID
- 114707406
- Publisher
- John Wiley and Sons
- Year
- 2012
- Tongue
- English
- Weight
- 252 KB
- Volume
- 167
- Category
- Article
- ISSN
- 0007-0963
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