Publication | Open Access
Cortical dysplasia resembling human type 2 lissencephaly in mice lacking all three APP family members
332
Citations
45
References
2004
Year
Developmental AnomalyKnockout MouseMolecular NeuroscienceDevelopmental BiologyBrain DevelopmentGenetic DisorderCorticobasal DegenerationHuman Type 2App Family MembersNeuroscienceNeurologyAbnormal DevelopmentNeuropathologyMedicineCortical DysplasiaSocial SciencesNeurogenetics
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