Investigating the Genetic Etiology of Pediatric Patients with Peripheral Hypotonia Using the Next-Generation Sequencing Method.

Eker, Damla; Gurkan, Hakan; Karal, Yasemin; Yalcintepe, Sinem; Demir, Selma; Atli, Engin; Karasalihoglu, Serap T

Eker, Damla; Gurkan, Hakan; Karal, Yasemin; Yalcintepe, Sinem; Demir, Selma; Atli, Engin; Karasalihoglu, Serap T.

Afiliación

Eker D; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey.
Gurkan H; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey.
Karal Y; Department of Pediatric Neurology, Faculty of Medicine, Trakya University, Edirne, Turkey.
Yalcintepe S; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey.
Demir S; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey.
Atli E; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey.
Karasalihoglu ST; Department of Pediatric Neurology, Faculty of Medicine, Trakya University, Edirne, Turkey.

Glob Med Genet ; 9(3): 200-207, 2022 Sep.

Article en En | MEDLINE | ID: mdl-35846108

Palabras clave

genetic etiology; hypotonia; multigene panel; next-generation sequencing; peripheral hypotonia

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Etiology_studies Idioma: En Revista: Glob Med Genet Año: 2022 Tipo del documento: Article País de afiliación: Turquía Pais de publicación: Alemania

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