✦ LIBER ✦
Lack ofNPHP2mutations in a newborn infant with Joubert syndrome-related disorder presenting as end-stage renal disease
✍ Scribed by Farahnak Assadi
- Publisher
- Springer
- Year
- 2007
- Tongue
- English
- Weight
- 92 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0931-041X
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