Pages that link to "Q50557392"

The following pages link to Characterization of a disease-causing Glu119-Lys mutation in the low-density lipoprotein receptor gene in two Danish families with heterozygous familial hypercholesterolemia (Q50557392):

Displaying 7 items.

• Identification of 13 new mutations in the vasopressin-neurophysin II gene in 17 kindreds with familial autosomal dominant neurohypophyseal diabetes insipidus (Q35882453) (← links)
• Complexity of molecular genetics of dyslipidemia in a family highly susceptible to ischemic heart disease (Q38293925) (← links)
• Software and database for the analysis of mutations in the human LDL receptor gene (Q39718607) (← links)
• A common W556S mutation in the LDL receptor gene of Danish patients with familial hypercholesterolemia encodes a transport-defective protein (Q50560640) (← links)
• Spectrum of LDL receptor gene mutations in Denmark: implications for molecular diagnostic strategy in heterozygous familial hypercholesterolemia (Q50564695) (← links)
• A sequence variation: 713-8delC in the transforming growth factor-beta 1 gene has higher prevalence in osteoporotic women than in normal women and is associated with very low bone mass in osteoporotic women and increased bone turnover in both osteop (Q73157670) (← links)
• Mutations in the low-density-lipoprotein receptor gene in German patients with familial hypercholesterolaemia (Q73482711) (← links)