NKX2-1 New Mutation Associated With Myoclonus, Dystonia, and Pituitary Involvement

Background: NKX2-1 related disorders (also known as brain-lung-thyroid syndrome or benign hereditary chorea 1) are associated with a wide spectrum of symptoms. The core features are various movement disorders, characteristically chorea, less frequently myoclonus, dystonia, ataxia; thyroid disease; a...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Pubblicato in:Front Genet
Autori principali: Balicza, Péter, Grosz, Zoltán, Molnár, Viktor, Illés, Anett, Csabán, Dora, Gézsi, Andras, Dézsi, Lívia, Zádori, Dénes, Vécsei, László, Molnár, Mária Judit
Natura: Artigo
Lingua:Inglês
Pubblicazione: Frontiers Media S.A. 2018
Soggetti:
Genetics
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6113386/
https://ncbi.nlm.nih.gov/pubmed/30186310
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2018.00335
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !

Documenti analoghi