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 (...

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Podrobná bibliografie

Hlavní autoři:	Valentina Peycheva, Neviana Ivanova, Kunka Kamenarova, Irina Tsekova, Iliyana Aleksandrova, Veneta Bozhinova, Maria Bozhidarova, Ivan Litvinenko, Dimitrina Hristova, Vanyo Mitev, Radka Kaneva, Albena Jordanova
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Taylor & Francis Group 2017-01-01
Edice:	Biotechnology & Biotechnological Equipment
Témata:	KCNQ2 mutations BFNS BFNIS BFIS 20q13.33 deletion
On-line přístup:	http://dx.doi.org/10.1080/13102818.2016.1259017
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