Clinical variability and female penetrance in X-linked familial FTD/ALS caused by a P506S mutation in UBQLN2. Vengoechea J, David MP, Yaghi SR, Carpenter L, Rudnicki SA Amyotroph Lateral Scler Frontotemporal Degener. 2013 Aug 14. PMID: 23944734. Abstract CommentRecommendBookmarkWatch