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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

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.

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Genre: Journal Article
Alternative Title : Cephalalgia

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Freilinger 22.4.08.pdf (Publisher version), 87KB
 
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Freilinger 22.4.08.pdf
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 Creators:
Freilinger, T., Author
Bohe, M., Author
Wegener, B., Author
Müller-Myhsok, B.1, Author           
Dichgans, M., Author
Knoblauch, H., Author
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1AG Müller-Myhsok, Bertram, Florian Holsboer (Direktor), Max Planck Institute of Psychiatry, Max Planck Society, ou_1607154              

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Language(s): eng - English
 Dates: 2008-04
 Publication Status: Issued
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 Identifiers: eDoc: 359306
ISI: 000253706600016
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Title: Cephalalgia
  Alternative Title : Cephalalgia
Source Genre: Journal
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Pages: - Volume / Issue: 28 (4) Sequence Number: - Start / End Page: 403 - 407 Identifier: ISSN: 0333-1024