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Genetic variants in TRPM7 associated with unexplained stillbirth modify ion channel function.
Cartwright, James H; Aziz, Qadeer; Harmer, Stephen C; Thayyil, Sudhin; Tinker, Andrew; Munroe, Patricia B.
Afiliação
  • Cartwright JH; Clinical Pharmacology, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ, UK.
  • Aziz Q; Clinical Pharmacology, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ, UK.
  • Harmer SC; Clinical Pharmacology, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ, UK.
  • Thayyil S; School of Physiology, Pharmacology and Neuroscience, Faculty of Life Sciences, The University of Bristol, Biomedical Sciences Building, University Walk, Bristol BS8 1TD, UK.
  • Tinker A; Centre for Perinatal Neuroscience, Imperial College London, London W12OHS, UK.
  • Munroe PB; Clinical Pharmacology, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ, UK.
Hum Mol Genet ; 29(11): 1797-1807, 2020 07 21.
Article em En | MEDLINE | ID: mdl-31423533

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Arritmias Cardíacas / Proteínas Serina-Treonina Quinases / Predisposição Genética para Doença / Canais de Cátion TRPM / Natimorto Tipo de estudo: Risk_factors_studies Limite: Animals / Humans Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Arritmias Cardíacas / Proteínas Serina-Treonina Quinases / Predisposição Genética para Doença / Canais de Cátion TRPM / Natimorto Tipo de estudo: Risk_factors_studies Limite: Animals / Humans Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Reino Unido