Home
About
Overview
Sharing Data
ORCID
Help
History (1)
Whole-Exome Sequencing Reveals CLCNKB Mutations in a Case of Sudden Unexpected Infant Death.
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
Whole-Exome Sequencing Reveals CLCNKB Mutations in a Case of Sudden Unexpected Infant Death.
Whole-Exome Sequencing Reveals CLCNKB Mutations in a Case of Sudden Unexpected Infant Death. Pediatr Dev Pathol. 2015 Jul-Aug; 18(4):324-6.
View in:
PubMed
subject areas
Autopsy
Bartter Syndrome
Cause of Death
Chloride Channels
DNA Mutational Analysis
Exome
Fatal Outcome
Genetic Predisposition to Disease
Humans
Infant, Newborn
Male
Mutation
Predictive Value of Tests
Sudden Infant Death
authors with profiles
Eden Haverfield