Identification of ANKDD1B variants in an ankylosing spondylitis pedigree and a sporadic patient.

Tan, Zhiping; Zeng, Hui; Xu, Zhaofa; Tian, Qi; Gao, Xiaoyang; Zhou, Chuanman; Zheng, Yu; Wang, Jian; Ling, Guanghui; Wang, Bing; Yang, Yifeng; Ma, Long

Tan, Zhiping; Zeng, Hui; Xu, Zhaofa; Tian, Qi; Gao, Xiaoyang; Zhou, Chuanman; Zheng, Yu; Wang, Jian; Ling, Guanghui; Wang, Bing; Yang, Yifeng; Ma, Long.

Afiliação

Tan Z; Clinical Center for Gene Diagnosis and Therapy, the Second Xiangya Hospital of Central South University, Changsha, 410011, China. zhipingtan@csu.edu.cn.
Zeng H; Department of Cardiovascular Surgery, the Second Xiangya Hospital of Central South University, Changsha, 410011, China. zhipingtan@csu.edu.cn.
Xu Z; Clinical Center for Gene Diagnosis and Therapy, the Second Xiangya Hospital of Central South University, Changsha, 410011, China.
Tian Q; Department of Cardiovascular Surgery, the Second Xiangya Hospital of Central South University, Changsha, 410011, China.
Gao X; Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, 410081, China.
Zhou C; Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, 410081, China.
Zheng Y; Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, 410081, China.
Wang J; Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, 410081, China.
Ling G; Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, 410081, China.
Wang B; Clinical Center for Gene Diagnosis and Therapy, the Second Xiangya Hospital of Central South University, Changsha, 410011, China.
Yang Y; Department of Cardiovascular Surgery, the Second Xiangya Hospital of Central South University, Changsha, 410011, China.
Ma L; Department of Rheumatology, the Second Xiangya Hospital of Cenral South University, Changsha, China.

BMC Med Genet ; 19(1): 111, 2018 07 05.

Article em En | MEDLINE | ID: mdl-29976160

Assuntos

Predisposição Genética para Doença/genética; Peptídeos e Proteínas de Sinalização Intracelular/genética; Mutação de Sentido Incorreto/genética; Espondilite Anquilosante/genética; Adolescente; Adulto; Aminoácidos/genética; Aminopeptidases/genética; Povo Asiático/genética; Estudos de Casos e Controles; Pré-Escolar; Estudos de Coortes; Feminino; Ligação Genética/genética; Haplótipos/genética; Humanos; Masculino; Antígenos de Histocompatibilidade Menor/genética; Linhagem; Receptores de Interleucina/genética; Adulto Jovem

Palavras-chave

ANKDD1B; Ankylosing spondylitis; Ankyrin repeat; HLA-B*27; Pedigree

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Espondilite Anquilosante / Predisposição Genética para Doença / Mutação de Sentido Incorreto / Peptídeos e Proteínas de Sinalização Intracelular Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child, preschool / Female / Humans / Male Idioma: En Revista: BMC Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China

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