Amanote Research
Register
Sign In
Connective Tissue Disorder Due to Lysyl Hydroxylase-3 Deficiency
doi 10.32388/ey7gr8
Full Text
Open PDF
Abstract
Available in
full text
Date
February 10, 2020
Authors
Unknown
Publisher
Qeios
Related search
A Connective Tissue Disorder Caused by Mutations of the Lysyl Hydroxylase 3 Gene
American Journal of Human Genetics
Genetics
Congenital Adrenal Hyperplasia Due to 11-Beta-Hydroxylase Deficiency
Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Lysyl Hydroxylase 3 Is a Multifunctional Protein Possessing Collagen Glucosyltransferase Activity
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
46,XY Disorder of Sex Development Due to 17-Beta-Hydroxysteroid Dehydrogenase 3 Deficiency
Psychological Vulnerability to Stress in Carriers of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Hormones
Medicine
Endocrinology
Metabolism
Diabetes
Corrigendum: Prolyl 3-Hydroxylase 1 Deficiency Causes a Recessive Metabolic Bone Disorder Resembling Lethal/Severe Osteogenesis Imperfecta
Nature Genetics
Genetics
Connective Tissue
Three Case Reports of Necrosis and Perforation of Intestine Due to Connective Tissue Disease.
Japanese Journal of Gastroenterological Surgery
Surgery
Gastroenterology
