CHCHD2 and Parkinson's disease

The Lancet Neurology

Volumn 14, Issue 7, 2015, Pages 681-682

  Foo, Jia Nee ^a   Liu, Jianjun ^a   Tan, Eng King ^b,c  

^a GENOME INSTITUTE OF SINGAPORE   (Singapore)

^b SINGAPORE GENERAL HOSPITAL   (Singapore)

^c DUKE NUS MEDICAL SCHOOL   (Singapore)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; CHCHD2 GENE; CHINESE; GENE; GENE MUTATION; GENOTYPE; HUMAN; JAPANESE (PEOPLE); LETTER; ONSET AGE; PARKINSON DISEASE; PRIORITY JOURNAL; DNA SEQUENCE; FEMALE; GENETIC ASSOCIATION; 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: 84930514845     PISSN: 14744422     EISSN: 14744465     Source Type: Journal    
DOI: 10.1016/S1474-4422(15)00098-8     Document Type: Letter

References (1)

1. Funayama M, Ohe K, Amo T, et al. CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study. Lancet Neurol 2015, 14:274-282.