Clinical variability and female penetrance in X-linked familial FTD/ALS caused by a P506S mutation in UBQLN2
Vengoechea, Jaime, David, Marjorie P., Yaghi, Shadi R., Carpenter, Lori, Rudnicki, Stacy A.Том:
14
Мова:
english
Журнал:
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
DOI:
10.3109/21678421.2013.824001
Date:
December, 2013
Файл:
PDF, 93 KB
english, 2013
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