M Muglia

2PUBLICATIONS
1CO-AUTHORS
Neurology and neuromuscular diseases
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Publications (2)

|May 28, 2020
A 71-nucleotide deletion in the periaxin gene in an Italian patient with late-onset slowly progressive demyelinating Charcot-Marie-Tooth disease.

L Citrigno, S Zoccolella, P Lastella

|Nov 10, 2018
Kinesins in neurological inherited diseases: a novel motor-domain mutation in KIF5A gene in a patient from Southern Italy affected by hereditary spastic paraplegia.

L Citrigno, A Magariello, P Pugliese

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I L Simone