A novel mutation in CDK5RAP2 gene causes primary microcephaly with speech impairment and sparse eyebrows in a consanguineous Pakistani family
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| Description | scientific article published on August 2017 |
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author: Klaus Wilbrandt Kjaer Ambrin Fatima Uzma Abdullah Lars A Larsen Shahid M Baig Syeda Marriam Bakhtiar Niels Tommerup |
| Publication date | August 1, 2017 |
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