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Nosel POMT2 mutations associated with a marked reduction of POMT activity causing congenital muscular dystrophy with mental retardation and microcephaly
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| Document type | Communication à un colloque (Conference Paper) |
|---|---|
| Access type | Accès restreint |
| Publication date | 2007 |
| Language | Anglais |
| Conference | "12th International Congress of the World-Muscle-Society", Giardini Naxos (Italy) (Oct 17-20, 2007) |
| Journal information | "Neuromuscular Disorders" - Vol. 17, no. 9-10, p. 870-870 (2007) |
| Peer reviewed | yes |
| issn | 0960-8966 |
| e-issn | 1873-2364 |
| Publisher | Pergamon-elsevier Science Ltd (Oxford) |
| Affiliations |
UCL
- Cliniques universitaires Saint-Luc UCL - MD/NOPS - Département de neurologie et de psychiatrie UCL - (SLuc) Service de neurologie |
| Links |
| Bibliographic reference | Yanagisawa, A. ; Van den Bergh, Peter ; Bouchet, C. ; Manya, H. ; Quijano-Roy, S. ; et. al. Nosel POMT2 mutations associated with a marked reduction of POMT activity causing congenital muscular dystrophy with mental retardation and microcephaly.12th International Congress of the World-Muscle-Society (Giardini Naxos (Italy), Oct 17-20, 2007). In: Neuromuscular Disorders, Vol. 17, no. 9-10, p. 870-870 (2007) |
|---|---|
| Permanent URL | http://hdl.handle.net/2078.1/59489 |