Clinical variability and female penetrance in X-linked familial FTD/ALS caused by a P506S mutation in UBQLN2

Author： Vengoechea Jaime David Marjorie P. Yaghi Shadi R. Carpenter Lori Rudnicki Stacy A.

ISSN： 2167-8421

Source： Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, Vol.14, Iss.7-8, 2013-12, pp. : 615-619

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