الوصف: Otoferlin Gene Mutation

العنوان بلغة أخرى:	الاختلال الوراثي في جين أوتوفيرلين
المؤلف الرئيسي:	Moharram Mohamed Khalil, Ghada
مؤلفين آخرين:	Nadia Mkamal (مشرف)
التاريخ الميلادي:	2010
الصفحات:	101
نوع المحتوى:	رسائل جامعية
اللغة:	الإنجليزية
الدرجة العلمية	رسالة ماجستير
الجامعة	Ain Shams University/Faculty of medicine
الدولة	مصر
المصدر:	غير محدد
الحالة	تمت المناقشة
قواعد المعلومات:	Thesis
المستخلص:	Identification of the underlying gene(s) for AN is one of the key challenges for understanding the molecular basis for different AN phenotypes. The genetic study of auditory neuropathy is complicated by the fact that the term includes hearing losses with
الوصف	Identification of the underlying gene(s) for AN is one of the key challenges for understanding the molecular basis for different AN phenotypes. The genetic study of auditory neuropathy is complicated by the fact that the term includes hearing losses with

خلاصة:	Identification of the underlying gene(s) for AN is one of the key challenges for understanding the molecular basis for different AN phenotypes. The genetic study of auditory neuropathy is complicated by the fact that the term includes hearing losses with
الوصف المادي:	101