Parkinson disease and clathrin coat dynamics at synapses, why not?

Movement Disorders

Volumn 32, Issue 8, 2017, Pages 1163-

  Saez Atienzar, Sara ^a   Singleton, Andrew B ^a  

^a NATIONAL INSTITUTE ON AGING   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

SYNAPTOJANIN; SYNAPTOJANIN 1; SYNAPTOSOMAL ASSOCIATED PROTEIN 25; UNCLASSIFIED DRUG; CLATHRIN; NERVE PROTEIN; PHOSPHATASE;

CLATHRIN-COATED VESICLE; ENDOCYTOSIS; IMMUNOFLUORESCENCE; MOTOR DYSFUNCTION; NONHUMAN; NOTE; PARKINSON DISEASE; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN DOMAIN; SYNAPSE; ULTRASTRUCTURE; AXON; HUMAN; MUTATION;

AXONS; CLATHRIN; HUMANS; MUTATION; NERVE TISSUE PROTEINS; PARKINSON DISEASE; PHOSPHORIC MONOESTER HYDROLASES; SYNAPSES;

EID: 85021821308     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.27097     Document Type: Note

References (6)

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2. Olgiati S, De Rosa A, Quadri M, et al. PARK20 caused by SYNJ1 homozygous Arg258Gln mutation in a new Italian family. Neurogenetics 2014;15(3):183-188.
3. Quadri M, Fang M, Picillo M, et al. Mutation in the SYNJ1 gene associated with autosomal recessive, early-onset Parkinsonism. Hum Mutat 2013;34(9):1208-1215.
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6. Olgiati S, Quadri M, Fang M, et al. DNAJC6 mutations associated with early-onset parkinson's disease. Ann Neurol 2016;79(2):244-256.