Home
About
Overview
Sharing Data
ORCID
Help
History (1)
Cortical dysplasia resembling human type 2 lissencephaly in mice lacking all three APP family members.
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
Cortical dysplasia resembling human type 2 lissencephaly in mice lacking all three APP family members.
Cortical dysplasia resembling human type 2 lissencephaly in mice lacking all three APP family members. EMBO J. 2004 Oct 13; 23(20):4106-15.
View in:
PubMed
subject areas
Amyloid beta-Protein Precursor
Animals
Animals, Newborn
Cerebral Cortex
Crosses, Genetic
Embryonic Development
Humans
Immunohistochemistry
Mice
Mice, Knockout
Mutation
Skull
Survival Rate
authors with profiles
Sangram S. Sisodia