Structural insights into Charcot–Marie–Tooth disease‐linked mutations in human GDAP1

Charcot–Marie–Tooth disease (CMT) is the most common inherited peripheral polyneuropathy in humans, and its different subtypes are linked to mutations in dozens of different genes. Mutations in ganglioside‐induced differentiation‐associated protein 1 (GDAP1) cause two types of CMT, demyelinating CMT...

Descripció completa

Dades bibliogràfiques

Autors principals:	Aleksi Sutinen, Giang Thi Tuyet Nguyen, Arne Raasakka, Gopinath Muruganandam, Remy Loris, Emil Ylikallio, Henna Tyynismaa, Luca Bartesaghi, Salla Ruskamo, Petri Kursula
Format:	Artigo
Idioma:	Inglês
Publicat:	Wiley 2022-07-01
Col·lecció:	FEBS Open Bio
Matèries:	Charcot–Marie–Tooth disease GDAP1 GST superfamily protein structure neuropathy stability
Accés en línia:	https://doi.org/10.1002/2211-5463.13422
Etiquetes:	Afegir etiqueta Sense etiquetes, Sigues el primer a etiquetar aquest registre!