De novo DNM1L mutation associated with mitochondrial epilepsy syndrome with fever sensitivity

Guardat en:
Dades bibliogràfiques
Publicat a:Neurol Genet
Autors principals: Ladds, Emma, Whitney, Andrea, Dombi, Eszter, Hofer, Monika, Anand, Geetha, Harrison, Victoria, Fratter, Carl, Carver, Janet, Barbosa, Ines A., Simpson, Michael, Jayawant, Sandeep, Poulton, Joanna
Format: Artigo
Idioma:Inglês
Publicat: Wolters Kluwer 2018
Matèries:
Clinical/Scientific Notes
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6089689/
https://ncbi.nlm.nih.gov/pubmed/30109270
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000258
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