P275: Complementary long-read sequencing to identify variants in neurological phenotypes

Genetics in Medicine Open 2026 Open access

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Authors: Carson C Smith, Güney Bademci, Shengru Guo, LéShon Peart, Nicholas A. Borja, Stephanie Bivona, Mustafa Said Tekin

DOI: 10.1016/j.gimo.2026.103769

Cited by: 0

Fields of Study & Subjects

Genomics and Rare Diseases Genomic variations and chromosomal abnormalities Genomics and Phylogenetic Studies