Hereditary glomerulopathy associated with a mitochondrial tRNA(Leu) gene mutation

Pediatric Nephrology

Volumn 13, Issue 6, 1999, Pages 477-480

  Cheong, Hae Ii ^a   Chae, Jong Hee ^a   Kim, Jung Sue ^a   Park, Hye Won ^b   Ha, Ii Soo ^a   Hwang, Yong Seung ^a   Lee, Hyun Soon ^c   Choi, Yong ^a  

^a Seoul National University Children's Hospital   (South Korea)

^b Seoul National University Boramae Hospital   (South Korea)

^c Seoul National University Hospital   (South Korea)

Author keywords

Alport syndrome; Diabetes; Focal segmental glomerulosclerosis; Hearing loss; MELAS syndrome

Indexed keywords

LEUCINE TRANSFER RNA; MITOCHONDRIAL RNA; STEROID;

ADOLESCENT; ALPORT SYNDROME; ARTICLE; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; DIABETES MELLITUS; DIFFERENTIAL DIAGNOSIS; DISEASE ASSOCIATION; FAMILY HISTORY; FEMALE; GENE MUTATION; GENETIC SCREENING; GLOMERULOPATHY; GLOMERULOSCLEROSIS; GLOMERULUS CAPILLARY; HEMATURIA; HUMAN; HUMAN TISSUE; KIDNEY FAILURE; MALE; MELAS SYNDROME; NEUROLOGIC EXAMINATION; NEUROMUSCULAR DISEASE; PRIORITY JOURNAL;

ADOLESCENT; BASEMENT MEMBRANE; CHILD; CHILD, PRESCHOOL; DNA, MITOCHONDRIAL; FEMALE; HEARING LOSS, SENSORINEURAL; HUMANS; INFANT; KIDNEY DISEASES; KIDNEY GLOMERULUS; MALE; MITOCHONDRIA; MITOCHONDRIA, MUSCLE; MUSCLE, SKELETAL; MUTATION; PEDIGREE; RNA, TRANSFER, LEU; SYNDROME;

EID: 0032804448     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004670050641     Document Type: Article

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