Impact of KCNQ2 mutations in Bulgarian patients with electroclinical syndromes with onset in the first year of life

Mutations in KCNQ2 are associated with a range of electroclinical syndromes with dominant inheritance that are differentiated by the age at onset of the seizures and are associated with good prognosis. These are benign familial neonatal seizures (BFNS), benign familial neonatal--infantile seizures (...

وصف كامل

التفاصيل البيبلوغرافية

المؤلفون الرئيسيون:	Valentina Peycheva, Neviana Ivanova, Kunka Kamenarova, Irina Tsekova, Iliyana Aleksandrova, Veneta Bozhinova, Maria Bozhidarova, Ivan Litvinenko, Dimitrina Hristova, Vanyo Mitev, Radka Kaneva, Albena Jordanova
التنسيق:	Artigo
اللغة:	Inglês
منشور في:	Taylor & Francis Group 2017-01-01
سلاسل:	Biotechnology & Biotechnological Equipment
الموضوعات:	KCNQ2 mutations BFNS BFNIS BFIS 20q13.33 deletion
الوصول للمادة أونلاين:	http://dx.doi.org/10.1080/13102818.2016.1259017
الوسوم:	إضافة وسم لا توجد وسوم, كن أول من يضع وسما على هذه التسجيلة!