A patient with congenital generalized lipodystrophy due to a novel mutation in BSCL2: indications for secondary mitchondrial dysfunction.
DSpace/Manakin Repository
A patient with congenital generalized lipodystrophy due to a novel mutation in BSCL2: indications for secondary mitchondrial dysfunction.
Jeninga, E.H.; de Vroede, M.; Hamers, N.; Breur, J.M.P.J.; Verhoeven - Duif, N.M.; Berger, R.M.F.; Kalkhoven, E.
(2012) Journal of Inherited Metabolic Disease, volume 4, pp. 47 - 54
(Article)
Download/Full Text
The full text of this publication is not available.
ISSN: 0141-8955
Publisher: Springer Netherlands
(Peer reviewed)
See
more statistics
about this item