CHCHD2 and Parkinson's disease

The Lancet Neurology

Volumn 14, Issue 7, 2015, Pages 679-680

  Liu, Guiyou ^a   Li, Keshen ^b  

^a Tianjin Airport Economic Area   (China)

^b GUANGDONG MEDICAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ALZHEIMER DISEASE; AUTOSOMAL DOMINANT INHERITANCE; CHCHD2 GENE; EUROPEAN; EXOME; GENE; GENE FREQUENCY; GENE MUTATION; GENETIC ASSOCIATION; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; HUMAN; HUMAN GENOME; JAPANESE (PEOPLE); LETTER; LINKAGE ANALYSIS; META ANALYSIS (TOPIC); PARKINSON DISEASE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; DNA SEQUENCE; FEMALE; GENETIC LINKAGE; GENETICS; MALE; MISSENSE MUTATION; PARKINSONISM; PROCEDURES;

MITOCHONDRIAL PROTEIN; TRANSCRIPTION FACTOR;

FEMALE; GENETIC LINKAGE; GENOME-WIDE ASSOCIATION STUDY; HUMANS; MALE; MITOCHONDRIAL PROTEINS; MUTATION, MISSENSE; PARKINSONIAN DISORDERS; SEQUENCE ANALYSIS, DNA; TRANSCRIPTION FACTORS;

EID: 84930510818     PISSN: 14744422     EISSN: 14744465     Source Type: Journal    
DOI: 10.1016/S1474-4422(15)00131-3     Document Type: Letter

References (10)

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