Literature DB >> 11082808

[Molecular diagnosis of hereditary neurologic diseases. Position paper].

T Gasser1, M Dichgans, K Jurkat-Rott, T Klockgether, T Klopstock, H Kretzschmar, F Lehmann-Horn, H Reichmann, A Rolfs, T Sander, F Stögbauer.   

Abstract

Entities:  

Mesh:

Year:  2000        PMID: 11082808     DOI: 10.1007/s001150050665

Source DB:  PubMed          Journal:  Nervenarzt        ISSN: 0028-2804            Impact factor:   1.214


× No keyword cloud information.
  1 in total

Review 1.  [Muscular atrophy as a symptom].

Authors:  J Schmiedel; H Reichmann
Journal:  Internist (Berl)       Date:  2004-10       Impact factor: 0.743

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.