
Phenotypic Variability in Fraternal Twins with PEX1 Mutations: Zellweger Syndrome with Discordant Clinical Phenotype
Author(s) -
Janet Simons
Publication year - 2013
Publication title -
hereditary genetics
Language(s) - English
Resource type - Journals
ISSN - 2161-1041
DOI - 10.4172/2161-1041.s5-001
Subject(s) - phenotype , zellweger syndrome , clinical phenotype , biology , genetics , gene , peroxisome