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Genet. 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"count": 0 } ], "sort_fields": [] } ] }, { "title": "Characterizing the molecular etiology of arthrogryposis multiplex congenita in patients with LGI4 mutations.", "journal": "Glia", "date": "2021", "authors": "Booth DG, Kozar N, Bradley S, Meijer D", "reference": { "type": "PubMed", "id": "34288120", "url": "https://pubmed.ncbi.nlm.nih.gov/34288120" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q8N135-1", "protein_name": "Leucine-rich repeat LGI family member 4", "gene_name": "LGI4", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "Q8N135", "url": "https://www.uniprot.org/uniprotkb/Q8N135" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.34288120", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": [ { "table_id": 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