Index Catalog // Hyrax

Filtrado por: Study Program Human Genetics and Genomics Study Program (HGSP)

Descripción:	Background: Single ventricle disease (SVD) is a subtype of congenital heart disease that frequently requires early staged surgical intervention for survival. It is well known that syndromic causes of SVD are associated with worse outcomes....
Fecha de Creacion:	August 1-2, 2024

Descripción:	Background: Alternating hemiplegia of childhood (AHC) is a rare condition most frequently caused by mutations in ATP1A3, encoding for the alpha-3 subunit of Na+/K+-ATPase, and D801N is the most common variant. Individuals with ATP1A3-D801N have...
Fecha de Creacion:	August 1-2, 2024

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