Mutations in ATP13A2 (PARK9) are associated with an...

Human Genomics 2019 / 12 Vol. 13; Iss. 1

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., Dion, Patrick A., Rouleau, Guy A., Daly, Mark J., Neale, Benjamin M., La Bella, Vincenzo, Katsanis, Nicholas
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Volume:
13
Language:
english
Journal:
Human Genomics
DOI:
10.1186/s40246-019-0203-9
Date:
December, 2019
File:
PDF, 1.81 MB
english, 2019
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