Novel Factor XIII variant identified through whole-genome sequencing in a child with intracranial hemorrhage.

Name: Novel Factor XIII variant identified through whole-genome sequencing in a child with intracranial hemorrhage.
Author: Briggs, Benjamin

Novel Factor XIII variant identified through whole-genome sequencing in a child with intracranial hemorrhage. — المؤلف: Briggs, Benjamin — Cold Spring Harbor molecular case studies 20190917

المؤلف: Briggs, Benjamin
النشر: Cold Spring Harbor molecular case studies 20190917
الموضوعات: Blood Coagulation Tests؛ Factor XIII؛ Factor XIII Deficiency؛ Hematoma؛ Humans؛ Infant؛ Intracranial Hemorrhages؛ KRIT1 Protein