Fatal congenital copper transport defect caused by a homozygous likely pathogenic variant of SLC31A1期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

Fatal congenital copper transport defect caused by a homozygous likely pathogenic variant of SLC31A1

Authors:	Christof Dame Denise Horn Lutz Schomburg Johannes Grünhagen Thilo Samson Chillon Anna Tietze Annika Vogt Christoph Bührer

Abstract:

Keywords:	cerebral hemorrhage ceruloplasmin copper CTR1 Menkes disease