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A novel splice site mutation in CEP135 is associated with primary microcephaly in a Pakistani family
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نویسنده
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Farooq Muhammad ,Fatima Ambrin ,Mang Yuan ,Hansen Lars ,Kjaer Klaus Wilbrandt ,Baig Shahid Mahmood ,Larsen Lars Allan ,Tommerup Niels
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منبع
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journal of human genetics - 2016 - دوره : 61 - شماره : 3 - صفحه:271 -273
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آدرس
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University of Copenhagen, Department of Cellular and Molecular Medicine, Denmark, National Institute for Biotechnology and Genetic Engineering (NIBGE)-PIEAS, Health Biotechnology Division, Human Molecular Genetics Laboratory, Faisalabad, Pakistan, University of Copenhagen, Department of Cellular and Molecular Medicine, Denmark, University of Copenhagen, Department of Cellular and Molecular Medicine, Denmark, University of Copenhagen, Department of Cellular and Molecular Medicine, Denmark, National Institute for Biotechnology and Genetic Engineering (NIBGE)-PIEAS, Health Biotechnology Division, Human Molecular Genetics Laboratory, Faisalabad, Pakistan, University of Copenhagen, Department of Cellular and Molecular Medicine, Denmark, University of Copenhagen, Department of Cellular and Molecular Medicine, Denmark
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Authors
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