A case report of two Moroccan patients with hereditary neurological disorders and molecular modeling study on the S72L de novo PMP22 variant

Hereditary neurological disorders represent a wild group of hereditary illnesses affecting mainly the nervous system, the majority of which have a Mendelian inheritance pattern. Here we present the case of two Moroccan patients each affected by a different hereditary neurological disorder. In the fi...

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Veröffentlicht in:	Revue neurologique 2023-10, Vol.179 (8), p.902-909
Hauptverfasser:	Ait El Cadi, C., Dafrallah, L., Amalou, G., Charif, M., Charoute, H., Araqi-Houssaini, A., Lakhiari, H., Lenaers, G., Barakat, A.
Format:	Artikel
Sprache:	eng
Schlagworte:	Aicardi-Goutières syndrome type 2 Charcot-Marie-Tooth type 3 Hereditary neurological disorders Life Sciences Moroccan patients Whole exome sequencing
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