Mpd Syndrome
Sept. 8, 2024
Scottish teenager, 18, reveals how he was diagnosed with ultra rare condition | Daily Mail Online POLD1 Germline Mutations in Patients Initially Diagnosed with Werner Syndrome - Lessel - 2015 - Human Mutation - Wiley Online Library PDF] Exome sequencing reveals a de novo POLD1 mutation causing phenotypic variability in mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome (MDPL). | Semantic Scholar Mpd Syndrome