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Paroxysmal myoglobinuria in a single family with carnitine palmitoyltransferase deficiency
Paroxysmal myoglobinuria in a single family with carnitine palmitoyltransferase deficiency
1996
R. Marconi
Moschini G
M. Villanova
B. Garavaglia
Paolo Corradini
A. Sabatino
G. Del Curatolo
G. Marchettini
Romagnoli Am
M. Agresti
Keywords:
Genetics
Biology
Carnitine palmitoyltransferase deficiency
Diabetes mellitus
Myoglobinuria
Endocrinology
Internal medicine
single family
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