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Molecular analysis of hyperoxaluria type 1 in Italian patients reveals eight new mutations in the alanine: glyoxylate aminotransferase gene.

PIRULLI D
•
PUZZER D
•
FERRETINI C
altro
FLORIAN, FIORELLA
1999
  • journal article

Periodico
HUMAN GENETICS
WOS
WOS:000081854000014
Archivio
http://hdl.handle.net/11368/2294943
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0032778022
Diritti
metadata only access
Soggetti
  • Alanine

  • Base Sequence

  • Exon

  • Gene Deletion

  • Human

  • Hyperoxaluria

  • Italy

  • Molecular Sequence Da...

  • Mutation

  • Point Mutation

  • Polymorphism

  • Genetic

  • Single-Stranded Confo...

  • Sequence Analysi

  • DNA

  • Transaminases

Scopus© citazioni
39
Data di acquisizione
Jun 7, 2022
Vedi dettagli
Visualizzazioni
3
Data di acquisizione
Apr 19, 2024
Vedi dettagli
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