Modification of CMT1 phenotypes by the independent coexisting neurogenetic disorders, McArdle disease and chromosome 5p trisomy

Florian P. Thomas, Thomas J. Geller, Angelika F. Hahn, Ludwig Gutmann, Xin Li Huang, Hui Wu, Herman E. Wyandt, Roger V. Lebo

Research output: Contribution to journalArticlepeer-review

Original languageEnglish (US)
Pages (from-to)472-476
Number of pages5
JournalAnnals of the New York Academy of Sciences
Volume883
DOIs
StatePublished - 1999
Externally publishedYes

ASJC Scopus subject areas

  • Neuroscience(all)
  • Biochemistry, Genetics and Molecular Biology(all)
  • History and Philosophy of Science

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