In vitro Identification of CACNA1H in the 9th Exon of Childhood Absence Epilepsy (CAE) Patients Using BioEdit and ClustalW2

Childhood absence epilepsy (CAE) is an autosomal dominant disorder and a heterogeneous familial condition in which family members express absence seizures initially and then show multiple phenotypes of myoclonic epilepsy, including partial or absence seizures and generalized tonic conic seizures. M...

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Dades bibliogràfiques

Autors principals:	Asma Irshad, Nadeem Sarwar, Halema Sadia, Muhammad Afzal, Mazhar Abbas, Sumaira Sharif, Saeeda Kalsoom, Amna Saeed
Format:	Artigo
Idioma:	Inglês
Publicat:	University of Management and Technology 2021-08-01
Col·lecció:	Bioscientific Review
Matèries:	DNA amplification epilepsy mutations prenatal diagnostic sequences
Accés en línia:	https://journals.umt.edu.pk/index.php/BSR/article/view/1557
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