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Authors: SANGIUOLO F BOTTA A MESORACA A SERVIDEI S MERLINI L FRATTA G NOVELLI G DALLAPICCOLA B
Citation: F. Sangiuolo et al., IDENTIFICATION OF 5 NEW MUTATIONS AND 3 NOVEL POLYMORPHISMS IN THE MUSCLE CHLORIDE CHANNEL GENE (CLCN1) IN 20 ITALIAN PATIENTS WITH DOMINANT AND RECESSIVE MYOTONIA-CONGENITA, Human mutation, 11(4), 1998, pp. 331-331

Authors: KAUKONEN JA AMATI P SUOMALAINEN A ROTIG A PISCAGLIA MG SALVI F WEISSENBACH J FRATTA G COMI G PELTONEN L ZEVIANI M
Citation: Ja. Kaukonen et al., AN AUTOSOMAL LOCUS PREDISPOSING TO MULTIPLE DELETIONS OF MTDNA ON CHROMOSOME 3P, American journal of human genetics, 58(4), 1996, pp. 763-769

Authors: ZEVIANI M AMATI P COMI G FRATTA G MARIOTTI C TIRANTI V
Citation: M. Zeviani et al., SEARCHING FOR GENES AFFECTING THE STRUCTURAL INTEGRITY OF THE MITOCHONDRIAL GENOME, Biochimica et biophysica acta. Molecular basis of disease, 1271(1), 1995, pp. 153-158

Authors: GRIFA A PIEMONTESE MR MELCHIONDA S ORIGONE P ZELANTE L COVIELLO D FRATTA G DALLAPICCOLA B BALESTRAZZI P AJMAR F GASPARINI P
Citation: A. Grifa et al., SCREENING OF NEUROFIBROMATOSIS TYPE-1 GENE - IDENTIFICATION OF A LARGE DELETION AND OF AN INTRONIC VARIANT, Clinical genetics, 47(6), 1995, pp. 281-284
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