Mutational analysis of SCN2B, SCN3B and SCN4B in a large Chinese Han family with generalized tonic–clonic seizure.
- Published in:
- Neurological Sciences, 2010, v. 31, n. 5, p. 675, doi. 10.1007/s10072-010-0390-6
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- Publication type:
- Article
Works matching DE "HAN family"
Results: 2
1
2
Identification of a novel loss-of-function mutation of the GLA gene in a Chinese Han family with Fabry disease.
- Published in:
- BMC Medical Genetics, 2018, v. 19, n. 1, p. N.PAG, doi. 10.1186/s12881-018-0734-2
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- Publication type:
- Article