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Three families sharing acyl-coA dehydrogenase 9 deficiency : from severe neonatal cardiomyopathy to ventricular hypertrophy diagnosed at 12 years
Primary tabs
Dewulf, Joseph P.
[UCL]
Barréa, Catherine
[UCL]
Vincent, Marie-Francoise
[UCL]
de laet, corinne
[ULB]
Van Coster, Rudy
[UZ Gent]
Marie, Sandrine
[UCL]
Nassogne, Marie-Cécile
[UCL]
Barréa, Catherine
[UCL]
Vincent, Marie-Francoise
[UCL]
de laet, corinne
[ULB]
Van Coster, Rudy
[UZ Gent]
Marie, Sandrine
[UCL]
Nassogne, Marie-Cécile
[UCL]
| Document type | Communication à un colloque (Conference Paper) – Poster |
|---|---|
| Access type | Accès interdit |
| Publication date | 2015 |
| Language | Anglais |
| Conference | "SSIEM", Lyon (du 01/09/2015 au 04/09/2015) |
| Journal information | "Journal of Inherited Metabolic Disease" - Vol. 38, no.Suppl1, p. S204 (september 2015) |
| Peer reviewed | yes |
| issn | 0141-8955 |
| e-issn | 1573-2665 |
| Publisher | Springer Netherlands ((Netherlands) Dordrecht) |
| Publication status | Publié |
| Affiliations |
UCL
- SSS/DDUV - Institut de Duve UCL - SSS/IONS/NEUR - Clinical Neuroscience UCL - (SLuc) Service de neurologie pédiatrique |
| Links |
| Bibliographic reference | Dewulf, Joseph P. ; Barréa, Catherine ; Vincent, Marie-Francoise ; de laet, corinne ; Van Coster, Rudy ; et. al. Three families sharing acyl-coA dehydrogenase 9 deficiency : from severe neonatal cardiomyopathy to ventricular hypertrophy diagnosed at 12 years.SSIEM (Lyon, du 01/09/2015 au 04/09/2015). In: Journal of Inherited Metabolic Disease, Vol. 38, no.Suppl1, p. S204 (september 2015) |
|---|---|
| Permanent URL | http://hdl.handle.net/2078.1/172100 |