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Volumn 8, Issue 7, 1997, Pages 1118-1124

Mutation in mitochondrial tRNA(Leu(UUR)) gene associated with progressive kidney disease

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

EID: 0030799145     PISSN: 10466673     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (109)

References (20)
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    • Van den Ouweland JMW, Lemkes HHPJ, Trembath RC, Ross R, Velho G, Cohen D, Froguel P, Maassen JA: Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA (leu(UUR)) gene. Diabetes 43: 746-751, 1994
    • (1994) Diabetes , vol.43 , pp. 746-751
    • Van Den Ouweland, J.M.W.1    Lemkes, H.H.P.J.2    Trembath, R.C.3    Ross, R.4    Velho, G.5    Cohen, D.6    Froguel, P.7    Maassen, J.A.8
  • 3
    • 0027369567 scopus 로고
    • Prevalence of mitochondrial gene mutations in families with diabetes mellitus
    • Vionnet N, Passa P, Froguel P: Prevalence of mitochondrial gene mutations in families with diabetes mellitus. Lancet 342: 1429-1430, 1993
    • (1993) Lancet , vol.342 , pp. 1429-1430
    • Vionnet, N.1    Passa, P.2    Froguel, P.3
  • 4
    • 84919260318 scopus 로고
    • Prevalence of maternally inherited diabetes and deafness in diabetic populations in the Netherlands
    • 't Hart LM, Lemkes HHPJ, Heine RJ, Stolk RP, Feskens EJ: Prevalence of maternally inherited diabetes and deafness in diabetic populations in the Netherlands [Letter]. Diabetologia 37: 1169, 1994
    • (1994) Diabetologia , vol.37 , pp. 1169
    • 'T Hart, L.M.1    Lemkes, H.H.P.J.2    Heine, R.J.3    Stolk, R.P.4    Feskens, E.J.5
  • 7
    • 0025666322 scopus 로고
    • Leu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
    • Leu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies. Nature 348: 651-653, 1990
    • (1990) Nature , vol.348 , pp. 651-653
    • Goto, Y.1    Nonaka, I.2    Horai, S.3
  • 8
    • 0021070402 scopus 로고
    • Use of single void urine samples to estimate quantitative proteinuria
    • Ginsberg JM, Chang BS, Matarese RA, Garella S: Use of single void urine samples to estimate quantitative proteinuria. N Engl J Med 309: 1543-1546, 1983
    • (1983) N Engl J Med , vol.309 , pp. 1543-1546
    • Ginsberg, J.M.1    Chang, B.S.2    Matarese, R.A.3    Garella, S.4
  • 11
    • 0029638664 scopus 로고
    • Mitochondrial DNA and disease
    • Johns DR: Mitochondrial DNA and disease. N Engl J Med 333: 638-644, 1995
    • (1995) N Engl J Med , vol.333 , pp. 638-644
    • Johns, D.R.1
  • 13
    • 0025314193 scopus 로고
    • Renal tubular involvement mimicking Bartter syndrome in a patient with Kearns-Sayre syndrome
    • Goto Y, Itami N, Kajii N, Tochimaru H, Endo M, Horai S: Renal tubular involvement mimicking Bartter syndrome in a patient with Kearns-Sayre syndrome. J Pediatr 116: 904-910, 1990
    • (1990) J Pediatr , vol.116 , pp. 904-910
    • Goto, Y.1    Itami, N.2    Kajii, N.3    Tochimaru, H.4    Endo, M.5    Horai, S.6
  • 16
    • 0026041854 scopus 로고
    • Congenital hypoplastic anemia, diabetes, and severe renal tubular dysfunction associated with a mitochondrial DNA deletion
    • Majander A, Suomalainen A, Vettenranta K, Suriola H, Perkkiö M, Holmberg C, Pihko H: Congenital hypoplastic anemia, diabetes, and severe renal tubular dysfunction associated with a mitochondrial DNA deletion. Pediatr Res 30: 327-330, 1991
    • (1991) Pediatr Res , vol.30 , pp. 327-330
    • Majander, A.1    Suomalainen, A.2    Vettenranta, K.3    Suriola, H.4    Perkkiö, M.5    Holmberg, C.6    Pihko, H.7
  • 17
    • 0026569283 scopus 로고
    • Maternally inherited duplication of the mitochondrial genome in a syndrome of proximal tubulopathy, diabetes mellitus, and cerebellar ataxia
    • Rötig A, Bessis JL, Romero N, Cormier V, Saudubay JM, Narcy P, Lenoir G, Rustin P, Munnich A: Maternally inherited duplication of the mitochondrial genome in a syndrome of proximal tubulopathy, diabetes mellitus, and cerebellar ataxia. Am J Hum Genet 50: 364-370, 1992
    • (1992) Am J Hum Genet , vol.50 , pp. 364-370
    • Rötig, A.1    Bessis, J.L.2    Romero, N.3    Cormier, V.4    Saudubay, J.M.5    Narcy, P.6    Lenoir, G.7    Rustin, P.8    Munnich, A.9
  • 19
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    • Complex I deficiency with diabetes, Fanconi syndrome and mtDNA deletion
    • Luder A, Barash V: Complex I deficiency with diabetes, Fanconi syndrome and mtDNA deletion. J Inherited Metab Dis 17: 298-300, 1994
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    • Luder, A.1    Barash, V.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.