PLA2G6 gene mutation and infantile neuroaxonal degeneration; report of three cases from Iran

OBJECTIVE(S): Infantile neuroaxonal degeneration (INAD) is a rare subgroup of neurodegeneration with brain iron accumulation (NBIA) disorders. This progressive disorder may develop during the early years of life. Affected individuals mostly manifest developmental delay and/or psychomotor regression...

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Detalles Bibliográficos
Autores principales: Jafarzadeh Esfehani, Reza, Eslahi, Atieh, Beiraghi Toosi, Mehran, Sadr-Nabavi, Ariane, Kerachian, Mohammad Amin, Asl Mohajeri, Mahsa Sadat, Farjami, Mahsa, Alizade, Farzaneh, Mojarrad, Majid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8751752/
https://www.ncbi.nlm.nih.gov/pubmed/35083005
http://dx.doi.org/10.22038/ijbms.2021.55082.12340

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8751752/
https://www.ncbi.nlm.nih.gov/pubmed/35083005
http://dx.doi.org/10.22038/ijbms.2021.55082.12340

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