GBA mutations and Parkinson disease: when genotype meets phenotype

Affiliations

¹ From the Department of Neurology (S.W.S.), Johns Hopkins Hospital, Baltimore; Laboratory of Neurogenetics (S.W.S.), National Institute on Aging, National Institutes of Health, Bethesda, MD; and Department of Neurology (B.S.J.), Seoul National University Hospital, Republic of Korea. sscholz5@jhmi.edu.
² From the Department of Neurology (S.W.S.), Johns Hopkins Hospital, Baltimore; Laboratory of Neurogenetics (S.W.S.), National Institute on Aging, National Institutes of Health, Bethesda, MD; and Department of Neurology (B.S.J.), Seoul National University Hospital, Republic of Korea.

Editorial

Sonja W Scholz et al. Neurology. 2015.

. 2015 Mar 3;84(9):866-7.

doi: 10.1212/WNL.0000000000001321. Epub 2015 Feb 4.

¹ From the Department of Neurology (S.W.S.), Johns Hopkins Hospital, Baltimore; Laboratory of Neurogenetics (S.W.S.), National Institute on Aging, National Institutes of Health, Bethesda, MD; and Department of Neurology (B.S.J.), Seoul National University Hospital, Republic of Korea. sscholz5@jhmi.edu.
² From the Department of Neurology (S.W.S.), Johns Hopkins Hospital, Baltimore; Laboratory of Neurogenetics (S.W.S.), National Institute on Aging, National Institutes of Health, Bethesda, MD; and Department of Neurology (B.S.J.), Seoul National University Hospital, Republic of Korea.

No abstract available

Comment on

Differential effects of severe vs mild GBA mutations on Parkinson disease.
Gan-Or Z, Amshalom I, Kilarski LL, Bar-Shira A, Gana-Weisz M, Mirelman A, Marder K, Bressman S, Giladi N, Orr-Urtreger A. Gan-Or Z, et al. Neurology. 2015 Mar 3;84(9):880-7. doi: 10.1212/WNL.0000000000001315. Epub 2015 Feb 4. Neurology. 2015. PMID: 25653295 Free PMC article.