✦ LIBER ✦
Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters
✍ Scribed by Victoria Harrison; Lyndsey Connell; Jesse Hayesmoore; Joanna McParland; Michael G. Pike; Edward Blair
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 391 KB
- Volume
- 155
- Category
- Article
- ISSN
- 1552-4825
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