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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Hlavní autoři:	Aleksi Sutinen, Giang Thi Tuyet Nguyen, Arne Raasakka, Gopinath Muruganandam, Remy Loris, Emil Ylikallio, Henna Tyynismaa, Luca Bartesaghi, Salla Ruskamo, Petri Kursula
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Wiley 2022-07-01
Edice:	FEBS Open Bio
Témata:	Charcot–Marie–Tooth disease GDAP1 GST superfamily protein structure neuropathy stability
On-line přístup:	https://doi.org/10.1002/2211-5463.13422
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