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Whole-Exome Sequencing Reveals Rare Germline Mutations in Patients With Hemifacial Microsomia
Hemifacial microsomia (HFM) is a rare congenital disease characterized by a spectrum of craniomaxillofacial malformations, including unilateral hypoplasia of the mandible and surrounding structures. Genetic predisposition for HFM is evident but the causative genes have not been fully understood. Thu...
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| Publicat a: | Front Genet |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Frontiers Media S.A.
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8165440/ https://ncbi.nlm.nih.gov/pubmed/34079577 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2021.580761 |
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