Variable penetrance of Andersen-Tawil syndrome in a family with a rare missense KCNJ2 mutation

Detalles Bibliográficos
Autores principales: Deeb, Reem, Veerapandiyan, Aravindhan, Tawil, Rabi, Treidler, Simona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2018
Materias:
Clinical/Scientific Notes
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244022/
https://www.ncbi.nlm.nih.gov/pubmed/30533530
http://dx.doi.org/10.1212/NXG.0000000000000284

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244022/
https://www.ncbi.nlm.nih.gov/pubmed/30533530
http://dx.doi.org/10.1212/NXG.0000000000000284

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