Authors:
He, Y
Jones, KJ
Vignier, N
Morgan, G
Chevallay, M
Barois, A
Estournet-Mathiaud, B
Hori, H
Mizuta, T
Tome, FMS
North, KN
Guicheney, P
Citation: Y. He et al., Congenital muscular dystrophy with primary partial laminin alpha 2 chain deficiency: Molecular study, NEUROLOGY, 57(7), 2001, pp. 1319-1322
Authors:
Labrune, P
Fabre, M
Trioche, P
Estournet-Mathiaud, B
Grangeponte, MC
Rambaud, C
Maurage, C
Bernard, O
Citation: P. Labrune et al., Jeune syndrome and liver disease: Report of three cases treated with ursodeoxycholic acid, AM J MED G, 87(4), 1999, pp. 324-328