M.P.1.06 A heterozygous Rapsyn (RAPSN) gene mutation (N88K) and (S201R), is a cause of progressive Limb Girdle Myasthenia

التفاصيل البيبلوغرافية
العنوان: M.P.1.06 A heterozygous Rapsyn (RAPSN) gene mutation (N88K) and (S201R), is a cause of progressive Limb Girdle Myasthenia
المؤلفون: Angela Abicht, L. Turon, Juliane Müller, Andrés Nascimento, D. Pascual-Vaca, Hanns Lochmüller, Jaume Colomer, Carlos Ortez
المصدر: Neuromuscular Disorders. 18:748-749
بيانات النشر: Elsevier BV, 2008.
سنة النشر: 2008
مصطلحات موضوعية: Genetics, Limb girdle myasthenia, Neurology, RAPSN gene, Pediatrics, Perinatology and Child Health, Mutation (genetic algorithm), Neurology (clinical), Biology, Genetics (clinical)
تدمد: 0960-8966
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::656c836cb8714da2293ddfa5870a67a6Test
https://doi.org/10.1016/j.nmd.2008.06.086Test
حقوق: CLOSED
رقم الانضمام: edsair.doi...........656c836cb8714da2293ddfa5870a67a6
قاعدة البيانات: OpenAIRE