Revue Neurologique
 2023
DOI: 10.1016/j.neurol.2023.01.728
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A case report of two Moroccan patients with hereditary neurological disorders and molecular modeling study on the S72L de novo PMP22 variant

Chaimaa Ait El Cadi
1
,
Loubna Dafrallah
2
,
Ghita Amalou
3
et al.
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