Syndrome of contiguous gene deletions in Xp-21 (deficiency of the glycerol-kinase complex). The association of Duchenne muscular dystrophy, glycerol kinase deficiency and congenital suprarenal hypoplasia
Casado de Frías, E, Ruibal Francisco, J L, Bueno Lozano, G, Pinel Simón, G, Reverte Blanc, F, Benítez Ortiz, J
Published in Anales españoles de pediatría (01.12.1997)
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Published in Anales españoles de pediatría (01.12.1997)
Journal Article