Xcode Life

Condition: HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 2

rs1085307096 in SLCO2A1 gene and HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 2

PMID 22906430 2012 Identification of mutations in the prostaglandin transporter gene SLCO2A1 and its phenotype-genotype correlation in Japanese patients with pachydermoperiostosis.

PMID 24929850 2014 The complete type of pachydermoperiostosis: a novel nonsense mutation p.E141* of the SLCO2A1 gene.

PMID 22553128 2012 Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis.

PMID 22197487 2012 Exome sequencing identifies SLCO2A1 mutations as a cause of primary hypertrophic osteoarthropathy.

PMID 22696055 2012 Mutations in the prostaglandin transporter SLCO2A1 cause primary hypertrophic osteoarthropathy with digital clubbing.

PMID 22331663 2012 Mutations in the prostaglandin transporter encoding gene SLCO2A1 cause primary hypertrophic osteoarthropathy and isolated digital clubbing.

PMID 24153155 2014 Three novel mutations in the SLCO2A1 gene in two Chinese families with primary hypertrophic osteoarthropathy.