PMC · DOI:10.1007/s12031-024-02233-3·June 1, 2024
Correction to: Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
Nesma M. Elaraby, Hoda A. Ahmed, Neveen A. Ashaat, Sameh Tawfik, Mahmoud K. H. Ahmed, Nehal F. Hassib, Engy A. Ashaat
Abstract
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Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
Diseases2
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TopicsConnective tissue disorders research · Peptidase Inhibition and Analysis · Ubiquitin and proteasome pathways