Skip to Main Content
CKG
Home
Home
Home
TKG
Paper Details
Breadcrumb
Paper Details
Paper Title
A novel mutation in CDK5RAP2 gene causes primary microcephaly with speech impairment and sparse eyebrows in a consanguineous Pakistani family.
PubMed
Paper Journal Title
Eur J Med Genet
Paper Citation Count
8
Paper Publication Year
2017
Bio Mention
Mesh Descriptor
Go
Actions
Author Name
Affiliation
Lars Allan Larsen
University of Copenhagen
1 - 1
Column Actions
Search
Datasets