Hearing loss mutations alter the functional properties of human P2X2 receptor channels through distinct mechanisms.

George, Benjamin; Swartz, Kenton J; Li, Mufeng

George, Benjamin; Swartz, Kenton J; Li, Mufeng.

Afiliação

George B; Molecular Physiology and Biophysics Section, Porter Neuroscience Research Center, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892-3701.
Swartz KJ; Molecular Physiology and Biophysics Section, Porter Neuroscience Research Center, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892-3701 kenton.swartz@nih.gov limuf@ninds.nih.gov.
Li M; Molecular Physiology and Biophysics Section, Porter Neuroscience Research Center, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892-3701 kenton.swartz@nih.gov limuf@ninds.nih.gov.

Proc Natl Acad Sci U S A ; 116(45): 22862-22871, 2019 11 05.

Article em En | MEDLINE | ID: mdl-31636190

Assuntos

Perda Auditiva/genética; Mutação; Receptores Purinérgicos P2X2/genética; Receptores Purinérgicos P2X2/fisiologia; Sequência de Aminoácidos; Humanos; Receptores Purinérgicos P2X2/química

Palavras-chave

ATP; cochlea; deafness; purinergic

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores Purinérgicos P2X2 / Perda Auditiva / Mutação Limite: Humans Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2019 Tipo de documento: Article

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