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Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration Volume 14, 2013 - Issue 7-8
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Research Article

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

Jaime VengoecheaDivision of Genetics, University of Arkansas for Medical Sciences College of Medicine, Little Rock, Arkansas, USACorrespondence[email protected]
,
Marjorie P. DavidDepartment of Pathology, University of Arkansas for Medical Sciences College of Medicine, Little Rock, Arkansas, USA
,
Shadi R. YaghiDepartment of Neurology, University of Arkansas for Medical Sciences College of Medicine, Little Rock, Arkansas, USA
,
Lori CarpenterDivision of Genetics, University of Arkansas for Medical Sciences College of Medicine, Little Rock, Arkansas, USA
&
Stacy A. RudnickiDepartment of Neurology, University of Arkansas for Medical Sciences College of Medicine, Little Rock, Arkansas, USA
Pages 615-619 | Received 07 Jun 2013, Accepted 07 Jul 2013, Published online: 14 Aug 2013

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