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Autor:
Marie Bruun, Lena Elisabeth Hjermind, Carsten Thomsen, Else Danielsen, Lise Lykke Thomsen, Lars Hageman Pinborg, Nastaran Khabbazbavani, Joergen Erik Nielsen
Publikováno v:
Case Reports in Neurology, Vol 7, Iss 1, Pp 84-89 (2015)
Familial hemiplegic migraine type 1 (FHM1), episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) are allelic disorders caused by mutations in the CACNA1A gene on chromosome 19p13. It is well described that FHM1 can present with cereb
Externí odkaz:
https://doaj.org/article/ffbb17137202433b8060794971c99855
