✦ LIBER ✦
A compound heterozygous missense mutation and a large deletion in the KCTD7 gene presenting as an opsoclonus-myoclonus ataxia-like syndrome
✍ Scribed by Blumkin, Lubov; Kivity, Sara; Lev, Dorit; Cohen, Sarit; Shomrat, Ruth; Lerman-Sagie, Tally; Leshinsky-Silver, Esther
- Book ID
- 118784404
- Publisher
- Springer
- Year
- 2012
- Tongue
- English
- Weight
- 620 KB
- Volume
- 259
- Category
- Article
- ISSN
- 0340-5354
No coin nor oath required. For personal study only.