Kristien Peeters

2PUBLICATIONS
9CO-AUTHORS
Neurology and neuromuscular diseasesNeurogenetics
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Publications (2)

|Sep 25, 2021
HINT1 founder mutation causing axonal neuropathy with neuromyotonia in South America: A case report.

Bianca de Aguiar Coelho Silva Madeiro, Kristien Peeters, Elker Lene Santos de Lima

|Mar 05, 2021
HINT1 neuropathy in Norway: clinical, genetic and functional profiling.

Silvia Amor-Barris, Helle Høyer, Lin V Brauteset

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Frequent Collaborators

2 joint publications

Silvia Amor-Barris

1 joint publications

Helle Høyer

1 joint publications

Lin V Brauteset

1 joint publications

Els De Vriendt