Reduced Cerebral White Matter Integrity Assessed by DTI in Cognitively Normal H63D-HFE Polymorphism Carriers

Author:

Meadowcroft Mark D.12ORCID,Wang Jianli2,Purnell Carson J.1,Eslinger Paul J.3,Neely Elizabeth B.1,Yang Qing X.12,Connor James R.1

Affiliation:

1. Department of Neurosurgery; The Pennsylvania State University - College of Medicine; Milton S. Hershey Medical Center; Hershey PA

2. Department of Radiology (Center for NMR Research); The Pennsylvania State University - College of Medicine; Milton S. Hershey Medical Center; Hershey PA

3. Department of Neurology; The Pennsylvania State University - College of Medicine; Milton S. Hershey Medical Center; Hershey PA

Funder

National Institutes of Health

Publisher

Wiley

Subject

Neurology (clinical),Radiology, Nuclear Medicine and imaging

Reference43 articles.

1. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis;Feder;Nat Genet,1996

2. H63D mutation in hemochromatosis alters cholesterol metabolism and induces memory impairment;Ali-Rahmani;Neurobiol Aging,2014

3. A global reference for human genetic variation;Auton;Nature,2015

4. An integrated map of structural variation in 2,504 human genomes;Sudmant;Nature,2015

5. HFE gene and hereditary hemochromatosis: a HuGE review;Hanson;Human Genome Epidemiology. Am J Epidemiol,2001

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