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A novel missense variant of the GNAI3 gene and recognisable morphological characteristics of the mandibula in ARCND1
Auriculocondylar syndrome (ARCND) is an autosomal monogenic disorder characterised by external ear abnormalities and micrognathia due to hypoplasia of the mandibular rami, condyle and coronoid process. Genetically, three subtypes of ARCND (ARCND1, ARCND2 and ARCND3) have been reported. To date, five...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Singapore
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8472909/ https://www.ncbi.nlm.nih.gov/pubmed/33723370 http://dx.doi.org/10.1038/s10038-021-00915-z |