Works matching IS 00223042 AND DT 2017 AND VI 143 AND IP 5


Results: 14
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    Issue Information.

    Published in:
    Journal of Neurochemistry, 2017, v. 143, n. 5, p. 455, doi. 10.1111/jnc.13824
    Publication type:
    Article
    9

    Issue Cover (December 2017).

    Published in:
    Journal of Neurochemistry, 2017, v. 143, n. 5, p. n/a, doi. 10.1111/jnc.13825
    Publication type:
    Article
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    Frequent genes in rare diseases: panel-based next generation sequencing to disclose causal mutations in hereditary neuropathies.

    Published in:
    Journal of Neurochemistry, 2017, v. 143, n. 5, p. 507, doi. 10.1111/jnc.14217
    By:
    • Dohrn, Maike F.;
    • Glöckle, Nicola;
    • Mulahasanovic, Lejla;
    • Heller, Corina;
    • Mohr, Julia;
    • Bauer, Christine;
    • Riesch, Erik;
    • Becker, Andrea;
    • Battke, Florian;
    • Hörtnagel, Konstanze;
    • Hornemann, Thorsten;
    • Suriyanarayanan, Saranya;
    • Blankenburg, Markus;
    • Schulz, Jörg B.;
    • Claeys, Kristl G.;
    • Gess, Burkhard;
    • Katona, Istvan;
    • Ferbert, Andreas;
    • Vittore, Debora;
    • Grimm, Alexander
    Publication type:
    Article
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