METABOLIC INVESTIGATION OF BANNAYAN-RILEY-RUVALCABA SYNDROME (BRRS), A PROGRESSIVE LIPID MYOPATHY
- 1 Anni 1997/1998
- 18.076€ Totale Fondi
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Pubblicazioni Scientifiche
- 1999 AMERICAN JOURNAL OF MEDICAL GENETICS
Long-chain L 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency does not appear to be the primary cause of lipid myopathy in patients with Bannayan-Riley-Ruvalcaba syndrome (ERRS)
- 1999 AMERICAN JOURNAL OF MEDICAL GENETICS
Long-chain L 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency does not appear to be the primary cause of lipid myopathy in patients with Bannayan-Riley-Ruvalcaba syndrome (BRRS).
