UBQLN2mutation causing heterogeneous X-linked dominant neurodegeneration

Author:

Fahed Akl C.1,McDonough Barbara12,Gouvion Cynthia M.3,Newell Kathy L.3,Dure Leon S.4,Bebin Martina4,Bick Alexander G.1,Seidman Jonathan G.1,Harter Donald H.5,Seidman Christine E.12

Affiliation:

1. Department of Genetics; Harvard Medical School; Boston MA

2. Cardiovascular Division and Howard Hughes Medical Institute, Brigham and Women's Hospital; Boston MA

3. Department of Pathology and Laboratory Medicine; University of Kansas Medical Center; Kansas City KS

4. Departments of Neurology and Pediatrics; University of Alabama at Birmingham; Birmingham AL

5. Department of Neurology; School of Medicine and Health Sciences, George Washington University; Washington DC

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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