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Details for article 4 of 14 found articles
| Title: |
Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6 |
| Author: |
Ratbi, Ilham Falkenberg, Kim D. Sommen, Manou Al-Sheqaih, Nada Guaoua, Soukaina Vandeweyer, Geert Urquhart, Jill E. Chandler, Kate E. Williams, Simon G. Roberts, Neil A. El Alloussi, Mustapha Black, Graeme C. Ferdinandusse, Sacha Ramdi, Hind Heimler, Audrey Fryer, Alan Lynch, Sally-Ann Cooper, Nicola Ong, Kai Ren Smith, Claire E.L. Inglehearn, Christopher F. Mighell, Alan J. Elcock, Claire Poulter, James A. Tischkowitz, Marc Davies, Sally J. Sefiani, Abdelaziz Mironov, Aleksandr A. Newman, William G. Waterham, Hans R. Van Camp, Guy |
| Appeared in: |
The American journal of human genetics |
| Paging: | Volume 97 (2015) nr. 4 pages 11 p. |
| Year: |
2015 |
| Contents: | |
| Publisher: |
The Authors |
| Source file: |
Elektronische Wetenschappelijke Tijdschriften |
Details for article 4 of 14 found articles
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