CNNM2 Heterozygous Variant Presenting as Hypomagnesemia and West Syndrome: Expanding the Spectrum of CNNM2 Gene-Related Epileptic Disorders

Detalles Bibliográficos
Autores principales: Panda, Prateek K., Lourembam, Radhapyari, Sharawat, Indar K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Letters to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8680880/
https://www.ncbi.nlm.nih.gov/pubmed/35002148
http://dx.doi.org/10.4103/aian.AIAN_1130_20

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8680880/
https://www.ncbi.nlm.nih.gov/pubmed/35002148
http://dx.doi.org/10.4103/aian.AIAN_1130_20

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