학술논문
Novel compound heterozygous variants (c.971delA/c.542C > T) in SLC1A4 causes spastic tetraplegia, thin corpus callosum, and progressive microcephaly: a case report and mutational analysis
Document Type
Article
Author
Source
In: Frontiers in Pediatrics . (Frontiers in Pediatrics, 12 July 2023, 11)
Subject
Language
English
ISSN
22962360