Search Results - R Croxen

  • Showing 1 - 2 results of 2
Refine Results
  1. 1
    Mutations in Different Functional Domains of the Human Muscle Acetylcholine Receptor Subunit in Patients with the Slow-Channel congenital Myasthenic Syndrome

    Mutations in Different Functional Domains of the Human Muscle Acetylcholine Receptor Subunit in Patients with the Slow-Channel congenital Myasthenic Syndrome by R Croxen, Claire Newland, David Beeson, Harry Oosterhuis, G Chauplannaz, Angela Vincent, John Newsom–Davis

    Published 1997
    Get full text
    Artigo
    Save to List
    Saved in:
  2. 2
    Correction: Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria

    Correction: Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria by Johannes N. Spelbrink, F.-Y Li, Valeria Tiranti, Kaisu Nikali, Qian Yuan, Muhammad Tariq, Sjoerd Wanrooij, N Garrido, Giacomo P. Comi, L. Morandi, Lucio Santoro, António Toscano, G Fabrizi, Hannu Somer, R Croxen, D Beeson, Joanna Poulton, Anu Suomalainen, Howard T. Jacobs, Massimo Zeviani, C. Larsson

    Published 2001
    Get full text
    Artigo
    Save to List
    Saved in:

Search Tools: