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Primary hypertrophic osteoarthropathy: Report of two novel genetic variants in the SLCO2A1 gene in two Mexican patients.

Indian journal of dermatology, venereology and leprology - 1 Jan 2000

Villarreal-Martínez Alejandra, Vázquez-Martínez Osvaldo T, Martínez-de-Villarreal Laura E, Garay-Mendoza Domingo, Rodríguez-Vivian Candelario, Ocampo-Candiani Jorge, De La Rosa-Marbán Edgar, Ibarra-Ramírez Marisol

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PMID: 29770782
DOI: 10.4103/ijdvl.IJDVL_414_17

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Related research

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Primary hypertrophic osteoarthropathy: Report of two novel genetic variants in the SLCO2A1 gene in two Mexican patients.PMID 29770782Read ↗

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Exome sequencing identifies SLCO2A1 mutations as a cause of primary hypertrophic osteoarthropathy.Semantic proximity Read ↗

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Genotype and phenotype characterization of primary hypertrophic osteoarthropathy type 2 and chronic enteropathy associated with SLCO2A1: Report of two cases and literature review.Semantic proximity Read ↗

Novel pathogenic variants in SLCO2A1 causing autosomal dominant primary hypertrophic osteoarthropathy.Semantic proximity Read ↗

Touraine-Solente-Gole syndrome: pathogenic variant in SLCO2A1 presented with polyarthralgia and digital clubbingSemantic proximity Read ↗

A novel mutation in the SLCO2A1 gene in a Chinese family with primary hypertrophic osteoarthropathy.Semantic proximity Read ↗

Primary hypertrophic osteoarthropathy: phenotypic variability and penetrance rate in heterozygotes for SLCO2A1 variantsSemantic proximity Read ↗

Mutations in the SLCO2A1 gene and primary hypertrophic osteoarthropathy: a clinical and biochemical characterization.Semantic proximity Read ↗

Primary hypertrophic osteoarthropathy with severe arthralgia identified by gene mutation of SLCO2A1.Semantic proximity Read ↗

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