@dpavot:29666464 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/@dpavot/sourceid/29666464","sourcedb":"@dpavot","sourceid":"29666464","source_url":"https://www.ncbi.nlm.nih.gov/pubmed/29666464","text":"We report a case with novel AARS2 gene mutations with developed striking cerebellar atrophy and leukoencephalopathy, which helps to further understand the clinical and genetic heterogeneity of AARS2-L.","tracks":[{"project":"PGR-UNK","denotations":[{"id":"T1","span":{"begin":28,"end":33},"obj":"57505"},{"id":"T2","span":{"begin":176,"end":189},"obj":"HP:0001425"}],"relations":[{"id":"R1","pred":"unknown","subj":"T1","obj":"T2"}],"attributes":[{"subj":"T1","pred":"source","obj":"PGR-UNK"},{"subj":"T2","pred":"source","obj":"PGR-UNK"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"PGR-UNK","color":"#ece693","default":true}]}]}}