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...

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Detalles Bibliográficos
Autores principales: Sutinen, Aleksi, Nguyen, Giang Thi Tuyet, Raasakka, Arne, Muruganandam, Gopinath, Loris, Remy, Ylikallio, Emil, Tyynismaa, Henna, Bartesaghi, Luca, Ruskamo, Salla, Kursula, Petri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249340/
https://www.ncbi.nlm.nih.gov/pubmed/35509130
http://dx.doi.org/10.1002/2211-5463.13422

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249340/
https://www.ncbi.nlm.nih.gov/pubmed/35509130
http://dx.doi.org/10.1002/2211-5463.13422

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