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A novel mutation in CDK5RAP2 gene causes primary microcephaly with speech impairment and sparse eyebrows in a consanguineous Pakistani family
Abdullah, Uzma, Farooq, Muhammad, Mang, Yuan, Marriam Bakhtiar, Syeda, Fatima, Ambrin, Hansen, Lars, Kjaer, Klaus Wilbrandt, Larsen, Lars Allan, Tommerup, Niels, Mahmood Baig, ShahidLanguage:
english
Journal:
European Journal of Medical Genetics
DOI:
10.1016/j.ejmg.2017.07.017
Date:
August, 2017
File:
PDF, 957 KB
english, 2017