Home
About
Overview
Sharing Data
ORCID
Help
History (5)
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria.
Editorial: Molecular diagnostics for infectious diseases: Novel approaches, clinical applications and future challenges.
Evaluation of the homogeneity of native T1 myocardial mapping using the polarity corrected inversion time preparation method in a myocardial phantom and healthy volunteers.
Monoallelic and biallelic mutations in RELN underlie a graded series of neurodevelopmental disorders.
Regenerative medicine and tissue engineering: contribution of stem cells in organ transplantation.
See All 5 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
Monoallelic and biallelic mutations in RELN underlie a graded series of neurodevelopmental disorders.
Monoallelic and biallelic mutations in RELN underlie a graded series of neurodevelopmental disorders. Brain. 2022 09 14; 145(9):3274-3287.
View in:
PubMed
subject areas
Adult
Cerebellum
Child
Developmental Disabilities
Humans
Lissencephaly
Mutation
Nervous System Malformations
authors with profiles
Sarah Keedy
Elliot S. Gershon
William B. Dobyns