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Identification of RELN variant p.(Ser2486Gly) in an Iranian family with ankylosing spondylitis; the first association of RELN and AS

30 Jan 2020

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 32001840
DOI: 10.1038/s41431-020-0573-4

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Identification of RELN variant p.(Ser2486Gly) in an Iranian family with ankylosing spondylitis; the first association of RELN and ASPMID 32001840Read ↗

Functional Analysis of RELN S2486G Mutation and its Contribution to Pathogenesis of Ankylosing Spondylitis.Semantic proximity Read ↗

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A study of the association between single nucleotide polymorphisms of the endoplasmic reticulum aminopeptidase 2 (ERAP2) gene and the risk of ankylosing spondylitis in Egyptians.Semantic proximity Read ↗

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