Renal manifestations of patients with MYH9-related disorders

Pediatric Nephrology

Volumn 26, Issue 4, 2011, Pages 549-555

  Han, Kyoung Hee ^a   Lee, Hyunkyung ^a   Kang, Hee Gyung ^a,b   Moon, Kyung Chul ^a,b   Lee, Joo Hoon ^c   Park, Young Seo ^c   Ha, Il Soo ^a   Ahn, Hyo Seop ^a   Choi, Yong ^d   Cheong, Hae Il ^a,b  

^a Seoul National University   (South Korea)

^b Seoul National University Hospital   (South Korea)

^c University of Ulsan College of Medicine   (South Korea)

^d Inje University College of Medicine   (South Korea)

Author keywords

Family history; Glomerulopathy; Motor domain; MYH9 gene; MYH9 related disorder; Non muscle myosin heavy chain IIA; Tail domain

Indexed keywords

MYOSIN HEAVY CHAIN; NON MUSCLE MYOSIN HEAVY CHAIN I; NON MUSCLE MYOSIN HEAVY CHAIN IIA; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ARTICLE; ASIAN; CATARACT; CELL INCLUSION; CHILD; CHRONIC KIDNEY DISEASE; CLINICAL ARTICLE; DISEASE COURSE; DISEASE SEVERITY; DOHLE LIKE BODY; FAMILY HISTORY; FEMALE; FOCAL GLOMERULOSCLEROSIS; GENE MUTATION; GENOTYPE; GENOTYPE PHENOTYPE CORRELATION; GLOMERULOSCLEROSIS; HEARING IMPAIRMENT; HEMATURIA; HUMAN; HUMAN TISSUE; INFANT; INTERSTITIAL NEPHRITIS; KIDNEY BIOPSY; KIDNEY DISEASE; KIDNEY DYSFUNCTION; KIDNEY FAILURE; MALE; MUTATIONAL ANALYSIS; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEINURIA; SCHOOL CHILD; THROMBOCYTE COUNT; THROMBOCYTOPENIA;

ADOLESCENT; ADULT; CEREBRAL INFARCTION; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; FEMALE; GENOTYPE; HEARING LOSS, SENSORINEURAL; HUMANS; INFANT; KIDNEY DISEASES; MALE; MOLECULAR MOTOR PROTEINS; MUTATION; MYOSIN HEAVY CHAINS; NEPHRITIS, HEREDITARY; PHENOTYPE; THROMBOCYTOPENIA;

EID: 79954445309     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00467-010-1735-3     Document Type: Article

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