Progressive Osseous Heteroplasia is not an Autosomal Dominant Trait but Reflects Superimposed Mosaicism in Different GNAS Inactivation Disorders

Progressive osseous heteroplasia (POH) is a rarely occurring genetic condition characterized by severe segmental ossification involving the skin and deep connective tissues including the muscles. So far, the disorder is generally described as an autosomal dominant trait. By contrast, the following a...

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Detalles Bibliográficos
Autor principal: Happle, Rudolf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Musings, Opinions, Tips and Experiences
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8088155/
https://www.ncbi.nlm.nih.gov/pubmed/33959533
http://dx.doi.org/10.4103/idoj.IDOJ_584_20

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8088155/
https://www.ncbi.nlm.nih.gov/pubmed/33959533
http://dx.doi.org/10.4103/idoj.IDOJ_584_20

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