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Titolo:
Isolated diffuse mesangial sclerosis and Wilms tumor suppressor gene
Autore:
Ito, S; Takata, A; Hataya, H; Ikeda, M; Kikuchi, H; Hata, J; Honda, M;
Indirizzi:
Tokyo Metropolitan Kiyose Childrens Hosp, Dept Nephrol, Tokyo, Japan TokyoMetropolitan Kiyose Childrens Hosp Tokyo Japan hrol, Tokyo, Japan Keio Univ, Sch Med, Dept Pathol, Tokyo 160, Japan Keio Univ Tokyo Japan 160 o Univ, Sch Med, Dept Pathol, Tokyo 160, Japan
Titolo Testata:
JOURNAL OF PEDIATRICS
fascicolo: 3, volume: 138, anno: 2001,
pagine: 425 - 427
SICI:
0022-3476(200103)138:3<425:IDMSAW>2.0.ZU;2-0
Fonte:
ISI
Lingua:
ENG
Soggetto:
FRASIER-SYNDROME; NEPHROTIC SYNDROME; MUTATIONS; WT1;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Clinical Medicine
Life Sciences
Citazioni:
13
Recensione:
Indirizzi per estratti:
Indirizzo: Ito, S Yokohama City Univ, Sch Med, Dept Pediat, Kanazawa Ku, 3-9 Fukuura,Yokohama, Kanagawa 2360004, Japan Yokohama City Univ 3-9 Fukuura Yokohama Kanagawa Japan 2360004 apan
Citazione:
S. Ito et al., "Isolated diffuse mesangial sclerosis and Wilms tumor suppressor gene", J PEDIAT, 138(3), 2001, pp. 425-427

Abstract

Diffuse mesangial sclerosis is a rare renal disease, occurring either in isolation or as part of Denys-Drash syndrome. Denys-Drash syndrome originates from mutations of the Wilms tumor suppressor gene (WT1). We describe the presence of WT1 mutations in 7 Japanese children with isolated diffuse mesangial sclerosis.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 31/03/20 alle ore 10:14:05