Rare Variants Analysis of Cutaneous Malignant Melanoma Genes in Parkinson’s Disease

Abstract A shared genetic susceptibility between cutaneous malignant melanoma (CMM) and Parkinson’s (PD) has been suggested. We investigated this by assessing the contribution of rare variants in genes involved in CMM to PD risk. We studied rare variation across 29 CMM risk genes using high quality...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Neurobiology of aging 2016-12, Vol.48, p.222.e1-222.e7
Hauptverfasser:	Lubbe, S.J, Escott-Price, V, Brice, A, Gasser, T, Pittman, A.M, Bras, J, Hardy, J, Heutink, P, Wood, N.M, Singleton, A.B, Grosset, D.G, Carroll, C.B, Law, M.H, Demenais, F, Iles, M.M, Bishop, D.T, Newton-Bishop, J, Williams, N.M, Morris, H.R
Format:	Artikel
Sprache:	eng
Schlagworte:	Cohort Studies Cutaneous malignant melanoma DCC Receptor Dopamine - biosynthesis Genetic Association Studies Genetic Predisposition to Disease - genetics Genetic Report Abstract Genetic Variation - genetics Genotype Humans Internal Medicine Melanins - biosynthesis Melanoma - genetics Membrane Glycoproteins - genetics Monophenol Monooxygenase Neurology Oxidoreductases - genetics Parkinson Disease - genetics Parkinson's Pigmentation Pigmentation - genetics Receptor, ErbB-4 - genetics Receptors, Cell Surface - genetics Risk Shared genetic background Skin Neoplasms - genetics Tumor Suppressor Proteins - genetics Tyrosinase Ubiquitin Thiolesterase - genetics
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Schreiben Sie den ersten Kommentar!