أعرض في EDS

G.P.10.08 Fetal myasthenia and arthrogryposis multiplex congenita caused by mutation in the fetal γ-subunit of the acetylcholine receptor (CHRNG): Escobar syndrome

التفاصيل البيبلوغرافية
العنوان: G.P.10.08 Fetal myasthenia and arthrogryposis multiplex congenita caused by mutation in the fetal γ-subunit of the acetylcholine receptor (CHRNG): Escobar syndrome
المؤلفون: V. Mihaylova, C. Fons, Andrés Nascimento, Juliane Müller, Jaume Colomer, Hanns Lochmüller, C. Jimenez-Mallabrera
المصدر: Neuromuscular Disorders. 17:820
بيانات النشر: Elsevier BV, 2007.
سنة النشر: 2007
مصطلحات موضوعية: Fetus, Arthrogryposis multiplex congenita, Neurology, Pediatrics, Perinatology and Child Health, Mutation (genetic algorithm), Escobar syndrome, Neurology (clinical), Biology, Molecular biology, Genetics (clinical), γ subunit, Acetylcholine receptor
تدمد: 0960-8966
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::c81642ceadfd9eba095e194cb66839b7Test
https://doi.org/10.1016/j.nmd.2007.06.199Test
حقوق: CLOSED
رقم الانضمام: edsair.doi...........c81642ceadfd9eba095e194cb66839b7
قاعدة البيانات: OpenAIRE
الوصف
تدمد:09608966