A novel splice site mutation in CEP135 is associated with primary microcephaly in a Pakistani family

Muhammad Farooq; Ambrin Fatima; Yuan Mang; Lars Hansen; Klaus Wilbrandt Kjaer; Shahid Mahmood Baig; Lars Allan Larsen; Niels Tommerup

doi:10.1038/jhg.2015.138

A novel splice site mutation in CEP135 is associated with primary microcephaly in a Pakistani family

Muhammad Farooq, Ambrin Fatima, Yuan Mang, Lars Hansen, Klaus Wilbrandt Kjaer, Shahid Mahmood Baig, Lars Allan Larsen, Niels Tommerup

Medical Genetics Program

Research output: Contribution to journal › Journal article › Research › peer-review

15 Citations (Scopus)

Original language	English
Journal	Journal of Human Genetics
Volume	61
Issue number	3
Pages (from-to)	271-273
Number of pages	3
ISSN	1434-5161
DOIs	https://doi.org/10.1038/jhg.2015.138
Publication status	Published - Mar 2016

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10.1038/jhg.2015.138

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A novel splice site mutation in CEP135 is associated with primary microcephaly in a Pakistani family. / Farooq, Muhammad; Fatima, Ambrin; Mang, Yuan; Hansen, Lars; Kjaer, Klaus Wilbrandt; Baig, Shahid Mahmood; Larsen, Lars Allan ; Tommerup, Niels.

In: Journal of Human Genetics, Vol. 61, No. 3, 03.2016, p. 271-273.

Research output: Contribution to journal › Journal article › Research › peer-review

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AU - Baig, Shahid Mahmood

AU - Larsen, Lars Allan

AU - Tommerup, Niels

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