Lack of association of a functional single nucleotide polymorphism of PTPN22, encoding lymphoid protein phosphatase, with susceptibility to Henoch-Schönlein purpura.
Year: 2007
Type: article
Study design: Observational Study
Source: PubMed
Institution: Consejo Superior de Investigaciones Científicas
Language: English
Subfield: Rheumatology
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W363915431
