PMC:5097349 / 7488-7771 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PMC/sourceid/5097349","sourcedb":"PMC","sourceid":"5097349","source_url":"https://www.ncbi.nlm.nih.gov/pmc/5097349","text":"The chromatograms of sequencing results. a The patient. b The daughter. c The control. In the area of the GFAP gene exon 8, there is a heterogeneous missense mutation point: c.1246C \u003e T (cytosine \u003e thymine, Aarrowhead), leading to amino acid change in p.R416W (arginine \u003e tryptophan)","tracks":[]}