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1دورية أكاديمية
المؤلفون: Mantuano, E, Trettel, F, Olsen, AS, Lennon, G, Frontali, M, IODICE, CARLA
المساهمون: Mantuano, E, Trettel, F, Olsen, A, Lennon, G, Frontali, M, Iodice, C
مصطلحات موضوعية: Oxidoreductases Acting on CH-NH Group Donor, Chromosome Mapping, Isoenzyme, Gene, Chromosomes, Human, Pair 19, Molecular Sequence Data, Exon, DNA, Complementary, Intron, Alternative Splicing, Settore BIO/18 - GENETICA
العلاقة: volume:215; issue:1; firstpage:153; lastpage:157; journal:GENE; http://hdl.handle.net/2108/46188Test
الإتاحة: https://doi.org/10.1016/S0378-1119Test(98)00254-6
http://hdl.handle.net/2108/46188Test -
2
المؤلفون: Veneziano L. 1, Guida S. 1, Mantuano E. 1, Bernard P. 1, Tarantino P. 2, Boccone L. 3, Hisama FM. 4, Carrera P. 5, Jodice C. 6,7, Frontali M. 1
المصدر: Journal of the neurological sciences 276 (2009): 31–37. doi:10.1016/j.jns.2008.08.030
info:cnr-pdr/source/autori:Veneziano L. 1; Guida S. 1; Mantuano E. 1;Bernard P. 1; Tarantino P. 2; Boccone L. 3; Hisama FM. 4; Carrera P. 5; Jodice C. 6,7; Frontali M. 1/titolo:Newly characterized 5' and 3' regions of CACNA1A gene harbour mutations associated with Familial Hemiplegic Migraine or episodic Ataxia type 2/doi:10.1016%2Fj.jns.2008.08.030/rivista:Journal of the neurological sciences/anno:2009/pagina_da:31/pagina_a:37/intervallo_pagine:31–37/volume:276مصطلحات موضوعية: Exon, Cerebral disorder, Central nervous system disease, Neurological disorder
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=cnr_________::ce23c3da06f211dc2ccb0772dd3e23cfTest
http://www.cnr.it/prodotto/i/4835Test -
3دورية أكاديمية
المؤلفون: Zanola, Annalisa, Parolini, Ornella
المساهمون: Wengler, G. S, Giliani, S, Fiorini, M, Mella, P, Mantuano, E, Zanola, Annalisa, Pollonini, G, Eibl, M. M, Ugazio, A. G, Notarangelo, L. D, Parolini, Ornella
مصطلحات موضوعية: DNA Mutational Analysi, Exon, Female, Frameshift Mutation, Genetic Testing, Human, Male, Pedigree, Point Mutation, Polymerase Chain Reaction, Prenatal Diagnosi, Receptors, Interleukin, Severe Combined Immunodeficiency, Mutation, Polymorphism, Single-Stranded Conformational, Settore BIO/13 - BIOLOGIA APPLICATA
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/9633906; info:eu-repo/semantics/altIdentifier/wos/WOS:000074236100030; volume:101; issue:3; firstpage:586; lastpage:591; numberofpages:6; issueyear:1998; journal:BRITISH JOURNAL OF HAEMATOLOGY; http://hdl.handle.net/10807/92504Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-7144261736