Format

Send to

Choose Destination
See comment in PubMed Commons below
J Med Genet. 2003 Jul;40(7):e87.

Phenotypic and genetic exploration of severe demyelinating and secondary axonal neuropathies resulting from GDAP1 nonsense and splicing mutations.

Author information

1
Inserm U491, Génétique Médicale et Développement, Faculté de Médecine la Timone, 13385 Marseille, France.
PMID:
12843336
PMCID:
PMC1735511
[Indexed for MEDLINE]
Free PMC Article
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for HighWire Icon for PubMed Central
    Loading ...
    Support Center