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Article

A case of Behcet's disease associated with myelodysplastic syndrome involving trisomy 8 and a gain-of-function mutation in SHP-2.

Rheumatology (Oxford, England) - 1 Jul 2011

Shigemura Tomonari, Agematsu Kazunaga, Yamazaki Takashi, Sakashita Kazuo, Nakayama Yoshiko, Higuchi Yumiko, Matsuda Kazuyuki, Koike Kenichi

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Share to Behcet Syndrome
Share to Chromosomes, Human, Pair 8
Share to Immunity, Innate

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Myelodysplastic Syndromes

Share to Protein Tyrosine Phosphatase, Non-Receptor Type 11

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Source

Identifiers

PMID: 21482541
DOI: 10.1093/rheumatology/ker137

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

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A case of Behcet's disease associated with myelodysplastic syndrome involving trisomy 8 and a gain-of-function mutation in SHP-2.PMID 21482541Read ↗

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