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Síndrome de Charcot-Marie-Tooth > Publicaciones

Mitochondrial defects and neuromuscular degeneration caused by altered expression of Drosophila Gdap1: implications for the Charcot–Marie–Tooth neuropathy

https://www.ncbi.nlm.nih.gov/pubmed/25122658
Por Víctor
Investigador

A Drosophila model of GDAP1 function reveals the involvement of insulin signalling in the mitochondria-dependent neuromuscular degeneration

https://www.ncbi.nlm.nih.gov/pubmed/28065847
Por Víctor
Investigador

Expanding the spectrum of genes responsible for hereditary motor neuropathies.J Neurol Neurosurg Psychiatry. 2019 Oct;90(10):1171-1179.

http://doi: 10.1136/jnnp-2019-320717. Epub 2019 Jun 5
Por Elena Pennisi
Investigador