ArticleEuropean journal of human genetics : EJHG2009

Noncanonical and canonical splice sites: a novel mutation at the rare noncanonical splice-donor cut site (IVS4+1A>G) of SEDL causes variable splicing isoforms in X-linked spondyloepiphyseal dysplasia tarda.

Feng Xiong et al.PubMed ↗Full text ↗Publisher ↗

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