Werner syndrome: identification of the homozygous g.nt 77177 a>g mutation(Genbank acc# AY44237) in the WRN gene in two apparently unrelated italian families from Sardinia suggests a founder effect / MASALA M; OLIVIERI C; PIRODDA C; COTTONI F; DANESINO C; CERIMELE D; SCAPPATICCI S. - (2005).

Werner syndrome: identification of the homozygous g.nt 77177 a>g mutation(Genbank acc# AY44237) in the WRN gene in two apparently unrelated italian families from Sardinia suggests a founder effect

COTTONI, Francesca Maria Giovanna;
2005

Werner syndrome: identification of the homozygous g.nt 77177 a>g mutation(Genbank acc# AY44237) in the WRN gene in two apparently unrelated italian families from Sardinia suggests a founder effect / MASALA M; OLIVIERI C; PIRODDA C; COTTONI F; DANESINO C; CERIMELE D; SCAPPATICCI S. - (2005).
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11388/135052
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact