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

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Standard

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.

I: Journal of Human Genetics, Bind 61, Nr. 3, 03.2016, s. 271-273.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Farooq, M, Fatima, A, Mang, Y, Hansen, L, Kjaer, KW, Baig, SM, Larsen, LA & Tommerup, N 2016, 'A novel splice site mutation in CEP135 is associated with primary microcephaly in a Pakistani family', Journal of Human Genetics, bind 61, nr. 3, s. 271-273. https://doi.org/10.1038/jhg.2015.138

APA

Farooq, M., Fatima, A., Mang, Y., Hansen, L., Kjaer, K. W., Baig, S. M., Larsen, L. A., & Tommerup, N. (2016). A novel splice site mutation in CEP135 is associated with primary microcephaly in a Pakistani family. Journal of Human Genetics, 61(3), 271-273. https://doi.org/10.1038/jhg.2015.138

Vancouver

Farooq M, Fatima A, Mang Y, Hansen L, Kjaer KW, Baig SM o.a. A novel splice site mutation in CEP135 is associated with primary microcephaly in a Pakistani family. Journal of Human Genetics. 2016 mar.;61(3):271-273. https://doi.org/10.1038/jhg.2015.138

Author

Farooq, Muhammad ; Fatima, Ambrin ; Mang, Yuan ; Hansen, Lars ; Kjaer, Klaus Wilbrandt ; Baig, Shahid Mahmood ; Larsen, Lars Allan ; Tommerup, Niels. / A novel splice site mutation in CEP135 is associated with primary microcephaly in a Pakistani family. I: Journal of Human Genetics. 2016 ; Bind 61, Nr. 3. s. 271-273.

Bibtex

@article{05f71eacea8c4c8eb788bf8ab82f5edc,
title = "A novel splice site mutation in CEP135 is associated with primary microcephaly in a Pakistani family",
author = "Muhammad Farooq and Ambrin Fatima and Yuan Mang and Lars Hansen and Kjaer, {Klaus Wilbrandt} and Baig, {Shahid Mahmood} and Larsen, {Lars Allan} and Niels Tommerup",
year = "2016",
month = mar,
doi = "10.1038/jhg.2015.138",
language = "English",
volume = "61",
pages = "271--273",
journal = "Journal of Human Genetics",
issn = "1434-5161",
publisher = "nature publishing group",
number = "3",

}

RIS

TY - JOUR

T1 - A novel splice site mutation in CEP135 is associated with primary microcephaly in a Pakistani family

AU - Farooq, Muhammad

AU - Fatima, Ambrin

AU - Mang, Yuan

AU - Hansen, Lars

AU - Kjaer, Klaus Wilbrandt

AU - Baig, Shahid Mahmood

AU - Larsen, Lars Allan

AU - Tommerup, Niels

PY - 2016/3

Y1 - 2016/3

U2 - 10.1038/jhg.2015.138

DO - 10.1038/jhg.2015.138

M3 - Journal article

C2 - 26657937

VL - 61

SP - 271

EP - 273

JO - Journal of Human Genetics

JF - Journal of Human Genetics

SN - 1434-5161

IS - 3

ER -

ID: 155607312