Found: 3
Select item for more details and to access through your institution.
The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies.
- Published in:
- Human Mutation, 2007, v. 28, n. 5, p. 522, doi. 10.1002/humu.9486
- By:
- Publication type:
- Article
Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutation.
- Published in:
- 2009
- By:
- Publication type:
- Letter
Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 3, p. 221, doi. 10.1093/hmg/10.3.221
- By:
- Publication type:
- Article