APA
Ehmke N., Graul-Neumann L., Smorag L., Koenig R., Segebrecht L., Magoulas P., Scaglia F., Kilic E., Hennig A. F., Adolphs N., Saha N., Fauler B., Kalscheuer V. M., Hennig F., Altmüller J., Netzer C., Thiele H., Nürnberg P., Yigit G., Jäger M., Hecht J., Krüger U., Mielke T., Krawitz P. M., Horn D., Schuelke M., Mundlos S., Bacino C. A., Bonnen P. E., Wollnik B., Fischer-Zirnsak B. & Kornak U. (20171113). De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction. : American journal of human genetics.
Chicago
Ehmke Nadja, Graul-Neumann Luitgard, Smorag Lukasz, Koenig Rainer, Segebrecht Lara, Magoulas Pilar, Scaglia Fernando, Kilic Esra, Hennig Anna F, Adolphs Nicolai, Saha Namrata, Fauler Beatrix, Kalscheuer Vera M, Hennig Friederike, Altmüller Janine, Netzer Christian, Thiele Holger, Nürnberg Peter, Yigit Gökhan, Jäger Marten, Hecht Jochen, Krüger Ulrike, Mielke Thorsten, Krawitz Peter M, Horn Denise, Schuelke Markus, Mundlos Stefan, Bacino Carlos A, Bonnen Penelope E, Wollnik Bernd, Fischer-Zirnsak Björn and Kornak Uwe. 20171113. De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction. : American journal of human genetics.
Harvard
Ehmke N., Graul-Neumann L., Smorag L., Koenig R., Segebrecht L., Magoulas P., Scaglia F., Kilic E., Hennig A. F., Adolphs N., Saha N., Fauler B., Kalscheuer V. M., Hennig F., Altmüller J., Netzer C., Thiele H., Nürnberg P., Yigit G., Jäger M., Hecht J., Krüger U., Mielke T., Krawitz P. M., Horn D., Schuelke M., Mundlos S., Bacino C. A., Bonnen P. E., Wollnik B., Fischer-Zirnsak B. and Kornak U. (20171113). De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction. : American journal of human genetics.
MLA
Ehmke Nadja, Graul-Neumann Luitgard, Smorag Lukasz, Koenig Rainer, Segebrecht Lara, Magoulas Pilar, Scaglia Fernando, Kilic Esra, Hennig Anna F, Adolphs Nicolai, Saha Namrata, Fauler Beatrix, Kalscheuer Vera M, Hennig Friederike, Altmüller Janine, Netzer Christian, Thiele Holger, Nürnberg Peter, Yigit Gökhan, Jäger Marten, Hecht Jochen, Krüger Ulrike, Mielke Thorsten, Krawitz Peter M, Horn Denise, Schuelke Markus, Mundlos Stefan, Bacino Carlos A, Bonnen Penelope E, Wollnik Bernd, Fischer-Zirnsak Björn and Kornak Uwe. De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction. : American journal of human genetics. 20171113.