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About this Neuroscience article

Absence of mutations in peripheral myelin protein-22, myelin protein zero, and connexin 32 in autosomal recessive Dejerine-Sottas syndrome by Florian Stögbauer; Peter Young; Heiko Wiebusch; Vincent Timmerman; Gregor Kuhlenbäumer; Eva Nelis; E.Bernd Ringelstein; Gerd Kurlemann; Gerd Assmann; Christine Van Broeckhoven; Harald Funke is a Neuroscience article available to read on EtoBox.

It is typically read by researchers, students, and practitioners in Neuroscience.

Author
Florian Stögbauer; Peter Young; Heiko Wiebusch; Vincent Timmerman; Gregor Kuhlenbäumer; Eva Nelis; E.Bernd Ringelstein; Gerd Kurlemann; Gerd Assmann; Christine Van Broeckhoven; Harald Funke
Publisher
Elsevier Science; Elsevier ; Elsevier BV (ISSN 0304-3940)
Published
1998
Language
EN
Field
Neuroscience (Life Sciences)

More by Florian Stögbauer; Peter Young; Heiko Wiebusch; Vincent Timmerman; Gregor Kuhlenbäumer; Eva Nelis; E.Bernd Ringelstein; Gerd Kurlemann; Gerd Assmann; Christine Van Broeckhoven; Harald Funke

Browse all works by Florian Stögbauer; Peter Young; Heiko Wiebusch; Vincent Timmerman; Gregor Kuhlenbäumer; Eva Nelis; E.Bernd Ringelstein; Gerd Kurlemann; Gerd Assmann; Christine Van Broeckhoven; Harald Funke