Browsing by Author "La Bella, Vincenzo"
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Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion
Spataro, Rossella; Kousi, Maria; Farhan, Sali M K; Willer, Jason R; Ross, Jay P; e.a. (BioMed Central, 2019-04-16)BACKGROUND: Amyotrophic lateral sclerosis [1] is a genetically heterogeneous neurodegenerative disorder, characterized by late-onset degeneration of motor neurons leading to progressive limb and bulbar weakness, as well ...