PMC:4157147 / 20621-20765 JSONTXT

Annnotations TAB JSON ListView MergeView

{"target":"https://pubannotation.org/docs/sourcedb/PMC/sourceid/4157147","sourcedb":"PMC","sourceid":"4157147","source_url":"https://www.ncbi.nlm.nih.gov/pmc/4157147","text":"(A and B) Sanger sequencing confirmed the presence of different homozygous missense mutations in GRHL2 in affected subjects from both pedigrees.","tracks":[]}