APA

Lahrouchi N., Lodder E. M., Mansouri M., Tadros R., Zniber L., Adadi N., Clur S. B., van Spaendonck-Zwarts K. Y., Postma A. V., Sefiani A., Ratbi I. & Bezzina C. R. (20170912). Exome sequencing identifies primary carnitine deficiency in a family with cardiomyopathy and sudden death. : European journal of human genetics : EJHG.

Chicago

Lahrouchi Najim, Lodder Elisabeth M, Mansouri Maria, Tadros Rafik, Zniber Layla, Adadi Najlae, Clur Sally-Ann B, van Spaendonck-Zwarts Karin Y, Postma Alex V, Sefiani Abdelaziz, Ratbi Ilham and Bezzina Connie R. 20170912. Exome sequencing identifies primary carnitine deficiency in a family with cardiomyopathy and sudden death. : European journal of human genetics : EJHG.

Harvard

Lahrouchi N., Lodder E. M., Mansouri M., Tadros R., Zniber L., Adadi N., Clur S. B., van Spaendonck-Zwarts K. Y., Postma A. V., Sefiani A., Ratbi I. and Bezzina C. R. (20170912). Exome sequencing identifies primary carnitine deficiency in a family with cardiomyopathy and sudden death. : European journal of human genetics : EJHG.

MLA

Lahrouchi Najim, Lodder Elisabeth M, Mansouri Maria, Tadros Rafik, Zniber Layla, Adadi Najlae, Clur Sally-Ann B, van Spaendonck-Zwarts Karin Y, Postma Alex V, Sefiani Abdelaziz, Ratbi Ilham and Bezzina Connie R. Exome sequencing identifies primary carnitine deficiency in a family with cardiomyopathy and sudden death. : European journal of human genetics : EJHG. 20170912.