[Updated on Apr. 18] Integration of CiNii Articles into CiNii Research

Congenital hypomyelinating neuropathy due to de novo heterozygous p. Asp6lAsn MPZ mutation: heterogeneous phenotypes caused by a single mutation in MPZ gene

Bibliographic Information

Title
Congenital hypomyelinating neuropathy due to de novo heterozygous p. Asp6lAsn MPZ mutation: heterogeneous phenotypes caused by a single mutation in MPZ gene
Author
Yonekawa T, Saito Y

Journal

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Details

  • CRID
    1010282257101583622
  • Article Type
    journal article
  • Data Source
    • KAKEN

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