A novel splice site mutation in CEP135 is associated with primary microcephaly in a Pakistani family
Muhammad Farooq1, Ambrin Fatima2, Yuan Mang1
1Wilhelm Johannsen Centre for Functional Genome Research, Department of Cellular and Molecular Medicine, University of Copenhagen, Copenhagen, Denmark.
Journal of Human Genetics
|December 15, 2015
Abstract
No abstract available in PubMed .
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