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pro vyhledávání: '"Mariam M. Mohsin"'
Autor:
Alian Fatima, Shahd A. Abuhijleh, Abdul Fatah, Mariam M. Mohsin, Subhranshu Sekhar Kar, Rajani Dube, Biji Thomas George, Manjunatha Goud Bellary Kuruba
Publikováno v:
Medicina, Vol 60, Iss 8, p 1322 (2024)
Infantile neuroaxonal dystrophy (INAD) is a rare neurodegenerative disorder affecting 1:1,000,000 children. It results from pathogenic variants in the PLA2G6 gene located on chromosome 22q13.1. The onset of symptoms usually occurs between 6 and 18 mo
Externí odkaz:
https://doaj.org/article/2ec5e3d4bbed4d93a2334c29a5071708
