Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Nastaran Khabbazbavani"'
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
Autor:
Lena E. Hjermind, Nastaran Khabbazbavani, Lise L Thomsen, Marie Bruun, Else R. Danielsen, Carsten Thomsen, Lars H. Pinborg, Joergen Erik Nielsen
Publikováno v:
Case Reports in Neurology, Vol 7, Iss 1, Pp 84-89 (2015)
Case Reports in Neurology
Case Reports in Neurology
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