Cystathionase deficiency in fibroblast cultures from a patient with primary cystathioninuria.

Ítems similars

• Deficiencies of cystathionase and homoserine dehydratase activities in cystathioninuria.
  per: Finkelstein, J D, et al.
  Publicat: (1966)
• Cystathioninuria from pyridoxine deficiency complicating treatment of hypercalcaemia in a cretin.
  per: Fourman, P., et al.
  Publicat: (1966)
• Glycopeptide storage in skin fibroblasts cultured from a patient with alpha-mannosidase deficiency.
  per: Tsay, G C, et al.
  Publicat: (1975)
• Deficiencies of fibrillin and decorin in fibroblast cultures of a patient with neonatal Marfan syndrome.
  per: Superti-Furga, A, et al.
  Publicat: (1992)
• Specific glutaryl-CoA dehydrogenating activity is deficient in cultured fibroblasts from glutaric aciduria patients.
  per: Hyman, D B, et al.
  Publicat: (1984)