Journal Article (Letter) DZNE-2020-04162

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Novel ATM mutation in a German patient presenting as generalized dystonia without classical signs of ataxia-telangiectasia.

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2015
Springer73057 Berlin

Journal of neurology 262(3), 768-770 () [10.1007/s00415-015-7636-4]

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Keyword(s): Ataxia Telangiectasia: genetics (MeSH) ; Ataxia Telangiectasia Mutated Proteins: genetics (MeSH) ; Dystonic Disorders: complications (MeSH) ; Dystonic Disorders: genetics (MeSH) ; Female (MeSH) ; Germany (MeSH) ; Humans (MeSH) ; Middle Aged (MeSH) ; Mutation: genetics (MeSH) ; Ataxia Telangiectasia Mutated Proteins

Classification:

Contributing Institute(s):
  1. Ext LMU Klinik (Ext LMU Klinik)
  2. Clinical Dementia Research München (Clinical Dementia Research München)
Research Program(s):
  1. 344 - Clinical and Health Care Research (POF3-344) (POF3-344)

Appears in the scientific report 2015
Database coverage:
Medline ; BIOSIS Previews ; Current Contents - Life Sciences ; Ebsco Academic Search ; IF < 5 ; JCR ; NCBI Molecular Biology Database ; SCOPUS ; Science Citation Index ; Science Citation Index Expanded ; Thomson Reuters Master Journal List ; Web of Science Core Collection
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Document types > Articles > Journal Article
Institute Collections > M DZNE > M DZNE-Ext LMU Klinik
Institute Collections > M DZNE > M DZNE-AG Levin
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 Record created 2020-02-18, last modified 2024-03-21



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