Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
September 1, 1995Neurology

Dejerine-Sottas disease with de novo dominant point mutation of the PMP22 gene

View Full Paper
Ask AI
Bookmark
Share

Authors

VIVictor IonâşescuIowa City Public LibraryRIR. IonasescuUniversity of IowaCSCh. SearbyUniversity of Iowa Hospitals and Clinics

Discussion

Loading...

Member takes

Implication

Key Points

Key points are not available for this paper at this time.

Cite This Study

Ionâşescu et al. (1995) studied this question.

synapsesocial.com/papers/6a9e84ffd8a839f6253800ebhttps://doi.org/10.1212/wnl.45.9.1766
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched one closely related paper. Consider it for comparative context:

  1. 1Autosomal recessive forms of hereditary motor and sensory neuropathy.1980 · 116 citations