✦ LIBER ✦
Chilren with ocular motor apraxia type Cogan carry deletions in the gene (NPHP1) for juvenile nephronopthisis
✍ Scribed by Regina Betz; Cornelia Rensing; Edgar Otto; Antoaneta Mincheva; Daniel Zebnder; Peter Lichter; Friedhelm Hildebrandt
- Book ID
- 117161592
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 820 KB
- Volume
- 136
- Category
- Article
- ISSN
- 1097-6833
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