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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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| Publicado no: | Exp Ther Med |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6090475/ https://ncbi.nlm.nih.gov/pubmed/30112060 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2018.6347 |
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