| dc.contributor.author | Lonnqvist, T. | |
| dc.contributor.author | Tyynismaa, H. | |
| dc.contributor.author | Ylikallio, E. | |
| dc.contributor.author | Woldegebriel, R. | |
| dc.contributor.author | Tumiati, M. | |
| dc.contributor.author | Isohanni, P. | |
| dc.contributor.author | Ryan, M. M. | |
| dc.contributor.author | Stark, Z. | |
| dc.contributor.author | Maie, W. | |
| dc.contributor.author | Sawyer, S. L. | |
| dc.contributor.author | Bell, K. M. | |
| dc.contributor.author | Oshlack, A. | |
| dc.contributor.author | Lockhart, P. L. | |
| dc.contributor.author | Shcherbii, M. | |
| dc.contributor.author | Estrada-Cuzcano, A. | |
| dc.contributor.author | Atkinson, D. | |
| dc.contributor.author | Hartley, T. | |
| dc.contributor.author | Tetreault, M. | |
| dc.contributor.author | Cuppen, I. | |
| dc.contributor.author | van der Pol, W. L. | |
| dc.contributor.author | Candayan, A. | |
| dc.contributor.author | Battaloglu, E. | |
| dc.contributor.author | van Gassen, K. L. I. | |
| dc.contributor.author | van den Boogaard, M. H. | |
| dc.contributor.author | Boycott, K. M. | |
| dc.contributor.author | Kauppi, L. | |
| dc.contributor.author | Jordanova, A. | |
| dc.contributor.author | Parman, Y. | |
| dc.date.accessioned | 2021-03-05T12:14:15Z | |
| dc.date.available | 2021-03-05T12:14:15Z | |
| dc.identifier.citation | Ylikallio E., Woldegebriel R., Tumiati M., Isohanni P., Ryan M. M. , Stark Z., Maie W., Sawyer S. L. , Bell K. M. , Oshlack A., et al., "MCM3AP in recessive axonal neuropathy and mild intellectual disability", 50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Danimarka, 27 - 30 Mayıs 2017, cilt.26, ss.40-41 | |
| dc.identifier.other | vv_1032021 | |
| dc.identifier.other | av_ac27ee70-e18e-46b0-8f23-4d9a2ecefa19 | |
| dc.identifier.uri | http://hdl.handle.net/20.500.12627/114889 | |
| dc.language.iso | eng | |
| dc.subject | GENETİK VE HAYAT | |
| dc.subject | BİYOKİMYA VE MOLEKÜLER BİYOLOJİ | |
| dc.subject | Moleküler Biyoloji ve Genetik | |
| dc.subject | Yaşam Bilimleri (LIFE) | |
| dc.subject | Tıbbi Genetik | |
| dc.subject | Yaşam Bilimleri | |
| dc.subject | Moleküler Biyoloji ve Genetik | |
| dc.subject | Sitogenetik | |
| dc.subject | Temel Bilimler | |
| dc.subject | Tıp | |
| dc.subject | Sağlık Bilimleri | |
| dc.subject | Dahili Tıp Bilimleri | |
| dc.title | MCM3AP in recessive axonal neuropathy and mild intellectual disability | |
| dc.type | Bildiri | |
| dc.contributor.department | University Of Helsinki , , | |
| dc.identifier.volume | 26 | |
| dc.contributor.firstauthorID | 154878 | |