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Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation

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http://pubman.mpdl.mpg.de/cone/persons/resource/persons80450

Müller-Myhsok,  B.
AG Müller-Myhsok, Bertram, Florian Holsboer (Direktor), Max Planck Institute of Psychiatry, Max Planck Society;

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Freilinger, T., Bohe, M., Wegener, B., Müller-Myhsok, B., Dichgans, M., & Knoblauch, H. (2008). Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation. Cephalalgia, 28(4), 403-407.


Cite as: http://hdl.handle.net/11858/00-001M-0000-000E-9456-7
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