Identification of a novel homozygous intron 3 splice site (A>T) mutation in the ARG1 gene in cerebral palsy pediatric cases from Odisha, India
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s11033-022-07499-7.pdf
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5. Cornelius LP, Raju V, Julin A (2019) Arginase deficiency presenting as acute encephalopathy. J Pediatr Neurosci 14(3):133
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