Genotype-phenotype correlation in the 5703G>A mutation in the tRNAAsn gene of mitochondrial DNA

被引:16
|
作者
Vives-Bauza, C
Del Toro, M
Solano, A
Montoya, J
Andreu, AL
Roig, M
机构
[1] Hosp Univ Vall Hebron, Seccio Neurol Infantil, Barcelona 08035, Spain
[2] Hosp Univ Vall Hebron, Ctr Invest Bioquim & Biol Mol, Barcelona 08035, Spain
[3] Univ Zaragoza, Dept Bioquim & Biol Mol, E-50009 Zaragoza, Spain
关键词
D O I
10.1023/A:1025133629685
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The 5703G>A mutation in the tRNA gene of mitochondrial DNA seems to show a tissue-specific phenotype: early age of clinical presentation, progressive external ophthalmoplegia, fatigability and 'extremely thin appearance'. We report a second patient with the same mutation and phenotype.
引用
收藏
页码:507 / 508
页数:2
相关论文
共 50 条
  • [21] Muscle phenotype and mutation load in 51 persons with the 3243A>G mitochondrial DNA mutation
    Jeppesen, Tina D.
    Schwartz, Marianne
    Frederiksen, Anja L.
    Wibrand, Flemming
    Olsen, David B.
    Vissing, John
    ARCHIVES OF NEUROLOGY, 2006, 63 (12) : 1701 - 1706
  • [22] A disease-associated G5703A mutation in the human mitochondrial DNA causes a conformational change and a marked disease in steady-state levels of the mitochondrial tRNAAsn.
    Hao, H
    Moraes, CT
    AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) : A310 - A310
  • [23] G507D mutation in FUS gene causes familial amyotrophic lateral sclerosis with a specific genotype-phenotype correlation
    Martinelli, Ilaria
    Zucchi, Elisabetta
    Pensato, Viviana
    Gellera, Cinzia
    Traynor, Bryan J.
    Gianferrari, Giulia
    Chio, Adriano
    Mandrioli, Jessica
    NEUROBIOLOGY OF AGING, 2022, 118 : 124 - 128
  • [24] Mutation Spectrum and Genotype-Phenotype Correlation in Cornelia de Lange Syndrome
    Mannini, Linda
    Cucco, Francesco
    Quarantotti, Valentina
    Krantz, Ian D.
    Musio, Antonio
    HUMAN MUTATION, 2013, 34 (12) : 1589 - 1596
  • [25] Cardiomyopathies due to mutations in the myopalladin gene: Genotype-phenotype correlation
    Purevjav, Enkhsaikhan
    Arimura, Takuro
    Augustin, Sibylle
    Nunoda, Shinichi
    Varela, Jaquelin
    Kearney, Debra L.
    McKenna, William
    Ackerman, Michael J.
    Kimura, Akinori
    Towbin, Jeffrey A.
    PROGRESS IN PEDIATRIC CARDIOLOGY, 2011, 31 (02) : 139 - +
  • [26] MUTATION SCREENING AND GENOTYPE-PHENOTYPE CORRELATION IN NF2 PATIENTS
    BOURN, D
    MASON, S
    TEKES, S
    CARTER, SA
    EVANS, DGR
    STRACHAN, T
    JOURNAL OF MEDICAL GENETICS, 1995, 32 (02) : 138 - 138
  • [27] Mutation spectrum and genotype-phenotype correlation of inherited retinal dystrophy in Taiwan
    Chen, Zhen-Ji
    Lin, Keng-Hung
    Lee, Shi-Huang
    Shen, Ren-Juan
    Feng, Zhuo-Kun
    Wang, Xiao-Fang
    Huang, Xiu-Feng
    Huang, Zhi-Qin
    Jin, Zi-Bing
    CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 2020, 48 (04): : 486 - 499
  • [28] Mutation screening and genotype-phenotype correlation in 32 families with Wilson disease
    Bost, M
    Lachaux, A
    Accominotti, M
    Vandenberghe, A
    JOURNAL OF TRACE ELEMENTS IN EXPERIMENTAL MEDICINE, 1999, 12 (04): : 321 - 329
  • [29] Distal hereditary motor neuropathies: Mutation spectrum and genotype-phenotype correlation
    Frasquet, Marina
    Rojas-Garcia, Ricard
    Argente-Escrig, Herminia
    Vazquez-Costa, Juan Francisco
    Muelas, Nuria
    Vilchez, Juan Jesus
    Sivera, Rafael
    Millet, Elvira
    Barreiro, Marisa
    Diaz-Manera, Jordi
    Turon-Sans, Janina
    Cortes-Vicente, Elena
    Querol, Luis
    Ramirez-Jimenez, Laura
    Martinez-Rubio, Dolores
    Sanchez-Monteagudo, Ana
    Espinos, Carmen
    Sevilla, Teresa
    Lupo, Vincenzo
    EUROPEAN JOURNAL OF NEUROLOGY, 2021, 28 (04) : 1334 - 1343
  • [30] Genotype-Phenotype Correlation in a New Fabry-Disease-Causing Mutation
    Cerkauskaite, Agne
    Cerkauskiene, Rimante
    Miglinas, Marius
    Laurinavicius, Arvydas
    Ding, Can
    Rolfs, Arndt
    Venceviciene, Lina
    Barysiene, Jurate
    Kazenaite, Edita
    Sadauskiene, Egle
    MEDICINA-LITHUANIA, 2019, 55 (05):