Le informazioni sugli articoli di fonte ISI sono coperte da copyright

Per ulteriori informazioni selezionare i riferimenti di interesse.

1. Engelbach, M; Forst, T; Hankeln, T; Tratzky, M; Heerdt, S; Pfutzner, A; Kann, P; Kunt, T; Schneider, S; Schmidt, ER; Beyer, J
   Germline mutations in the MEN1 gene: Creation of a new splice acceptor site and insertion of 7 intron nucleotides into the mRNA
   INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
   
   M. Engelbach et al., "Germline mutations in the MEN1 gene: Creation of a new splice acceptor site and insertion of 7 intron nucleotides into the mRNA", INT J MOL M, 4(5), 1999, pp. 483-485
2. Gudayol, M; Vidal-Taboada, JM; Usac, EF; Costa, A; Cristobal, P; dell'Anna, C; Oliva, R; Gomis, R
   Detection of a new variant of the mitochondrial glycerol-3-phosphate dehydrogenase gene in Spanish type 2 DM patients
   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
   
   M. Gudayol et al., "Detection of a new variant of the mitochondrial glycerol-3-phosphate dehydrogenase gene in Spanish type 2 DM patients", BIOC BIOP R, 263(2), 1999, pp. 439-445
3. LI M; KUIVENHOVEN JA; AYYOBI AF; PRITCHARD PH
   T-]G OR T-]A MUTATION INTRODUCED IN THE BRANCHPOINT CONSENSUS SEQUENCE OF INTRON-4 OF LECITHIN-CHOLESTEROL ACYLTRANSFERASE (LCAT) GENE - INTRON RETENTION CAUSING LCAT DEFICIENCY
   Biochimica et biophysica acta, L. Lipids and lipid metabolism
   
   M. Li et al., "T-]G OR T-]A MUTATION INTRODUCED IN THE BRANCHPOINT CONSENSUS SEQUENCE OF INTRON-4 OF LECITHIN-CHOLESTEROL ACYLTRANSFERASE (LCAT) GENE - INTRON RETENTION CAUSING LCAT DEFICIENCY", Biochimica et biophysica acta, L. Lipids and lipid metabolism, 1391(2), 1998, pp. 256-264