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Understanding the role of genetic variability in LRRK2 in Indian population.
Download from api.wiley.comDe novo FBXO11 mutations are associated with intellectual disability and behavioural anomalies
UploadClinical and genetic characteristics of sporadic adult-onset degenerative ataxia
UploadHypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia
UploadA comprehensive quality control workflow for paired tumor-normal NGS experiments
Download from academic.oup.comSeqPurge: highly-sensitive adapter trimming for paired-end NGS data
Download from doi.orgGuidelines for diagnostic next-generation sequencing
Download from www.nature.comTargeted 46-gene and clinical exome sequencing for mutations causing cardiomyopathies
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