دورية أكاديمية

Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions

التفاصيل البيبلوغرافية
العنوان: Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions
المؤلفون: Montse Olivé, Martin Engvall, Gianina Ravenscroft, Macarena Cabrera-Serrano, Hong Jiao, Carlo Augusto Bortolotti, Marcello Pignataro, Matteo Lambrughi, Haibo Jiang, Alistair R. R. Forrest, Núria Benseny-Cases, Stefan Hofbauer, Christian Obinger, Gianantonio Battistuzzi, Marzia Bellei, Marco Borsari, Giulia Di Rocco, Helena M. Viola, Livia C. Hool, Josep Cladera, Kristina Lagerstedt-Robinson, Fengqing Xiang, Anna Wredenberg, Francesc Miralles, Juan José Baiges, Edoardo Malfatti, Norma B. Romero, Nathalie Streichenberger, Christophe Vial, Kristl G. Claeys, Chiara S. M. Straathof, An Goris, Christoph Freyer, Martin Lammens, Guillaume Bassez, Juha Kere, Paula Clemente, Thomas Sejersen, Bjarne Udd, Noemí Vidal, Isidre Ferrer, Lars Edström, Anna Wedell, Nigel G. Laing
المصدر: Nature Communications, Vol 10, Iss 1, Pp 1-14 (2019)
بيانات النشر: Nature Portfolio
سنة النشر: 2019
المجموعة: Directory of Open Access Journals: DOAJ Articles
مصطلحات موضوعية: Science
الوصف: Myoglobin is a hemeprotein that reversibly binds oxygen and gives muscle its red color. Here, the authors report a genetic variant in the MB gene that associates with myoglobinopathy, an autosomal dominant progressive myopathy, and altered oxygen binding properties of the mutant protein.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 2041-1723
العلاقة: https://doi.org/10.1038/s41467-019-09111-2Test; https://doaj.org/toc/2041-1723Test; https://doaj.org/article/66b676bb69fb44be94c22654e712d730Test
DOI: 10.1038/s41467-019-09111-2
الإتاحة: https://doi.org/10.1038/s41467-019-09111-2Test
https://doaj.org/article/66b676bb69fb44be94c22654e712d730Test
رقم الانضمام: edsbas.415F0FF0
قاعدة البيانات: BASE
الوصف
تدمد:20411723
DOI:10.1038/s41467-019-09111-2