Mutations in galactosemia.

Ítems similars

• Molecular basis of galactosemia: mutations and polymorphisms in the gene encoding human galactose-1-phosphate uridylyltransferase.
  per: Reichardt, J K, et al.
  Publicat: (1991)
• Molecular characterization of two galactosemia mutations: correlation of mutations with highly conserved domains in galactose-1-phosphate uridyl transferase.
  per: Reichardt, J K, et al.
  Publicat: (1991)
• Molecular analysis of 11 galactosemia patients.
  per: Reichardt, J K
  Publicat: (1991)
• A common mutation associated with the Duarte galactosemia allele.
  per: Elsas, L. J., et al.
  Publicat: (1994)
• Molecular characterization of mutations in galactosemia genes: structural and functional implications
  per: Singh, R, et al.
  Publicat: (2014)