Authors:
De Kremer, RD
Paschini-Capra, A
Bacman, S
Argarana, C
Civallero, G
Kelley, RI
Guelbert, N
Latini, A
de Halac, IN
Giner-Ayala, A
Johnston, J
Proujansky, R
Gonzalez, I
Depetris-Boldini, C
Oller-Ramirez, A
Angaroni, C
Theaux, RA
Hliba, E
Juaneda, E
Citation: Rd. De Kremer et al., Barth's syndrome-like disorder: A new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation), AM J MED G, 99(2), 2001, pp. 83-93
Authors:
Depetris-Boldini, C
Galetto, R
Videla, MP
Dodelson, RD
Citation: C. Depetris-boldini et al., Increased excretion of coproporphyrin I in a patient with hereditary tyrosinaemia type I: Relevant changes with NTBC treatment, J INH MET D, 22(3), 1999, pp. 227-230