Home
About
Overview
Sharing Data
ORCID
Help
History (1)
De novo variants in HK1 associated with neurodevelopmental abnormalities and visual impairment.
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
De novo variants in HK1 associated with neurodevelopmental abnormalities and visual impairment.
De novo variants in HK1 associated with neurodevelopmental abnormalities and visual impairment. Eur J Hum Genet. 2019 07; 27(7):1081-1089.
View in:
PubMed
subject areas
Adolescent
Adult
Child
Erythrocytes
Female
Hereditary Sensory and Motor Neuropathy
Hexokinase
Humans
Infant
Male
Mutation, Missense
Pedigree
Retinitis Pigmentosa
authors with profiles
Peter Hulick