Infantile neuroaxonal dystrophy caused by PLA2G6 gene mutation in a Chinese patient: A case report

Infantile neuroaxonal dystrophy (INAD) is a rare neurodegenerative disorder. Phospholipase A2 group VI (PLA2G6) gene mutations have been identified in the majority of individuals with INAD. The present case report is on a Chinese female pediatric patient (age, 18 months) diagnosed with INAD with dea...

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Detalles Bibliográficos
Autores principales: Wang, Baotian, Wu, De, Tang, Jiulai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090475/
https://www.ncbi.nlm.nih.gov/pubmed/30112060
http://dx.doi.org/10.3892/etm.2018.6347

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090475/
https://www.ncbi.nlm.nih.gov/pubmed/30112060
http://dx.doi.org/10.3892/etm.2018.6347

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