Zobrazeno 1 - 1
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pro vyhledávání: '"Sameera F. Qureshi"'
Autor:
Sameera F. Qureshi, Altaf Ali, Venkateshwari Ananthapur, M.P. Jayakrishnan, Narasimhan Calambur, Kumarasamy Thangaraj, Pratibha Nallari
Publikováno v:
Indian Heart Journal, Vol 65, Iss 5, Pp 552-560 (2013)
Background: Autosomal recessive Long QT syndrome is characterized by prolonged QTc along with congenital bilateral deafness depends on mutations in K+ channel genes. A family of a Long QT syndrome proband from India has been identified with novel ind
Externí odkaz:
https://doaj.org/article/a0fe3c91cae94a15aa3fd47ea66fc488
