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Chiari Malformation Type I in a Patient with a Novel NKX2-1 Mutation
Chiari Malformation Type 1 is a congenital, condition characterized by abnormally shaped cerebellar tonsils that are displaced below the level of the foramen magnum. NKX2-1 gene encodes a transcription factor expressed during early development of thyroid, lung, and forebrain, and germline NKX2-1 mut...
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| Publicado no: | J Pediatr Neurosci |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer - Medknow
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6798275/ https://ncbi.nlm.nih.gov/pubmed/31649781 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/jpn.JPN_108_18 |
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