Home
About
Overview
Sharing Data
ORCID
Help
History (1)
Mutations in SCO2 are associated with autosomal-dominant high-grade myopia.
See All Pages
Find People
Find Everything
Login
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
0
)
Return to Top
Mutations in SCO2 are associated with autosomal-dominant high-grade myopia.
Mutations in SCO2 are associated with autosomal-dominant high-grade myopia. Am J Hum Genet. 2013 May 02; 92(5):820-6.
View in:
PubMed
subject areas
Animals
Animals
Base Sequence
Base Sequence
Carrier Proteins
Carrier Proteins
Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 22
Codon, Nonsense
Codon, Nonsense
Copper
Copper
Exome
Exome
Gene Expression Regulation
Gene Expression Regulation
Genes, Dominant
Genes, Dominant
Genetic Predisposition to Disease
Genetic Predisposition to Disease
Humans
Humans
Immunohistochemistry
Immunohistochemistry
Mice
Mice
Mitochondrial Proteins
Mitochondrial Proteins
Molecular Chaperones
Molecular Chaperones
Molecular Sequence Data
Molecular Sequence Data
Myopia
Myopia
Point Mutation
Point Mutation
RNA, Messenger
RNA, Messenger
Sequence Analysis, DNA
Sequence Analysis, DNA
United States
United States
authors with profiles
Tammy L Yanovitch