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Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypes.

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المؤلفون: Schymick, J C; Yang, Y; Andersen, P M; Vonsattel, J P; Greenway, M; Momeni, P; Elder, J; Chiò, A; Restagno, G; Robberecht, W; Dahlberg, C; Mukherjee, O; Goate, A; Graff-Radford, N; Caselli, R J; Hutton, M; Gass, J; Cannon, A; Rademakers, R; Singleton, A B; Hardiman, O; Rothstein, J; Hardy, J; Traynor, B J
نوع التسجيلة:
Electronic Resource
الدخول الالكتروني :
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-10689
J Neurol Neurosurg Psychiatry, 1468-330X, 2007, 78:7, s. 754-6

معلومة اضافية
- Publisher Information:
  Umeå universitet, Neurologi 2007
- الموضوع:
  Adult; Aged; Aged; 80 and over; Amyotrophic Lateral Sclerosis/*complications/*genetics; Cross-Sectional Studies; DNA Mutational Analysis; Dementia/*etiology/*genetics; Female; Humans; Intercellular Signaling Peptides and Proteins/*genetics; Male; Middle Aged; Mutation; Missense; Phenotype; Article in journal; info:eu-repo/semantics/article; text
- الرقم المعرف:
  10.1136.jnnp.2006.109553
- Availability:
  Open access content. Open access content
  info:eu-repo/semantics/restrictedAccess
- Note:
  English
- Other Numbers:
  UPE oai:DiVA.org:umu-10689
  doi:10.1136/jnnp.2006.109553
  PMID 17371905
  1233446699
- Contributing Source:
  UPPSALA UNIV LIBR
  From OAIster®, provided by the OCLC Cooperative.
- الرقم المعرف:
  edsoai.on1233446699

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