Monoallelic mutations in SLCO2A1 cause autosomal dominant primary hypertrophic osteoarthropathy.

Xu, Yang; Zhang, Zeng; Yue, Hua; Li, Shanshan; Zhang, Zhenlin

Xu, Yang; Zhang, Zeng; Yue, Hua; Li, Shanshan; Zhang, Zhenlin.

Afiliação

Xu Y; Shanghai Clinical Research Center of Bone Disease, Department of Osteoporosis and Bone Diseases, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
Zhang Z; Shanghai Clinical Research Center of Bone Disease, Department of Osteoporosis and Bone Diseases, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
Yue H; Shanghai Clinical Research Center of Bone Disease, Department of Osteoporosis and Bone Diseases, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
Li S; Shanghai Clinical Research Center of Bone Disease, Department of Osteoporosis and Bone Diseases, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
Zhang Z; Shanghai Clinical Research Center of Bone Disease, Department of Osteoporosis and Bone Diseases, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.

J Bone Miner Res ; 36(8): 1459-1468, 2021 08.

Article em En | MEDLINE | ID: mdl-33852188

Assuntos

Transportadores de Ânions Orgânicos; Osteoartropatia Hipertrófica Primária; Variações do Número de Cópias de DNA; Etoricoxib; Humanos; Mutação/genética; Transportadores de Ânions Orgânicos/genética; Osteoartropatia Hipertrófica Primária/genética; Linhagem

Palavras-chave

AUTOSOMAL DOMINANT PRIMARY HYPERTROPHIC OSTEOARTHROPATHY; ETORICOXIB; MONOALLELIC MUTATIONS; PGE2; SLCO2A1

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteoartropatia Hipertrófica Primária / Transportadores de Ânions Orgânicos Limite: Humans Idioma: En Revista: J Bone Miner Res Assunto da revista: METABOLISMO / ORTOPEDIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China País de publicação: Estados Unidos

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