The American Journal of Human Genetics
Volume 102, Issue 2, 1 February 2018, Pages 219-232
ArticleLoss of GPNMB Causes Autosomal-Recessive Amyloidosis Cutis Dyschromica in Humans
Under an Elsevier user license
open archive
Keywords
amyloidosis cutis dyschromica
amyloid
GPNMB
Glycoprotein nonmetastatic gene B
hyperpigmentation
hypopigmentation
DBA/2J
glaucoma
pigment dispersion
PMEL
Cited by (0)
© 2017 American Society of Human Genetics.