Mutational Analysis of the RET and GDNF Gene in Children with Hypoganglionosis
Kyoko Inoue(University Hospital Kyoto Prefectural University of Medicine), N. Iwai(Kyoto Prefectural University of Medicine), Takashi Shimotake(Kyoto Prefectural University of Medicine), Hiroyuki Tomiyama(German Center for Neurodegenerative Diseases)
Cited by 23
Related Papers
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
|Nature Genetics|2009|1.3k
CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study
|The Lancet Neurology|2015|359
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study
|The Lancet Neurology|2011|344
Clinical heterogeneity of α‐synuclein gene duplication in Parkinson's disease
|Annals of Neurology|2005|314