1986
DOI: 10.1001/archderm.122.1.76
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Hereditary deficiency of C2 in association with linear scleroderma 'en coup de sabre'

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“…Other non-HLA genes which are likely factors in the pathogenesis of the disease are: the protein tyrosine phosphatase nonreceptor 22 (PTPN22), interleukin (IL)-1b and NLRP1, interferon regulatory factor 5 (IRF5), and a transcription factor in the Toll-like receptor (TLR) [ 16 18 ]. Additionally, the downregulation of microRNA let-7a is thought to contribute to the excessive production of collagen in localized scleroderma [ 14 ].…”
Section: Hereditary Disease?
mentioning
confidence: 99%