Mutation (genetics) < Mutation (physiology) < Mutation, Missense

Facettes :

List of bibliographic references indexed by Mutation (physiology)

Number of relevant bibliographic references: 6.

Ident.	Authors (with country if any)	Title
000867 (2013)	Mitra Ansari Dezfouli [Iran] ; Afagh Alavi ; Mohammad Rohani ; Mohamad Rezvani ; Tayebeh Nekuie ; Brandy Klotzle ; Seyed Hasan Tonekaboni ; Gholam Ali Shahidi ; Elahe Elahi	PANK2 and C19orf12 mutations are common causes of neurodegeneration with brain iron accumulation.
000A96 (2013)	Annika Plate [Allemagne] ; Jens Benninghoff ; Gerald H. Jansen ; Elisabeth Wlasich ; Sabina Eigenbrod ; Alexander Drzezga ; Nathalie L. Jansen ; Hans A. Kretzschmar ; Kai Bötzel ; Dan Rujescu ; Adrian Danek	Atypical parkinsonism due to a D202N Gerstmann-Sträussler-Scheinker prion protein mutation: first in vivo diagnosed case.
000A98 (2013)	Claude Vital [France] ; Anne Vital	Are substantia nigra neurons subject to mitochondrial dysfunction in early life more able to adapt?
002219 (2009)	Bart F. L. Van Nuenen [Pays-Bas, Allemagne] ; Thilo Van Eimeren [Canada] ; Joyce P. M. Van Der Vegt [Pays-Bas, Allemagne] ; Carsten Buhmann [Allemagne] ; Christine Klein [Allemagne] ; Bastiaan R. Bloem [Pays-Bas] ; Hartwig R. Siebner [Allemagne, Danemark]	Mapping preclinical compensation in Parkinson's disease: An imaging genomics approach
002277 (2009)	Christine Klein [Allemagne, Canada] ; Susanne A. Schneider [Allemagne, Royaume-Uni] ; Anthony E. Lang [Canada]	Hereditary parkinsonism: Parkinson disease look‐alikes—An algorithm for clinicians to “PARK” genes and beyond
004E20 (1999)	Oscar Joost [États-Unis] ; Catherine A. Taylor [États-Unis] ; Catherine A. Thomas [États-Unis] ; L. Adrienne Cupples [États-Unis] ; Marie H. Saint-Hilaire [États-Unis] ; Robert G. Feldman [États-Unis] ; Clinton T. Baldwin [États-Unis] ; Richard H. Myers [États-Unis]	Absence of effect of seven functional mutations in the cyp2d6 gene in Parkinson's disease

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