Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis

Kidney International

Volumn 81, Issue 1, 2012, Pages 94-99

  Gbadegesin, Rasheed A ^a   Lavin, Peter J ^a   Hall, Gentzon ^a   Bartkowiak, Bartlomiej ^a   Homstad, Alison ^a   Jiang, Ruiji ^a   Wu, Guanghong ^a   Byrd, Alison ^a   Lynn, Kelvin ^b   Wolfish, Norman ^c   Ottati, Carolina ^d   Stevens, Paul ^e   Howell, David ^a   Conlon, Peter ^f   Winn, Michelle P ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

^b CHRISTCHURCH HOSPITAL   (New Zealand)

^c CHILDREN S HOSPITAL OF EASTERN ONTARIO   (Canada)

^d Centrode Nefrologia Hospital de Clinicus Dr Manuel Quintela ^*  (Uruguay)

^e EAST KENT HOSPITALS UNIVERSITY NHS FOUNDATION TRUST   (United Kingdom)

^f BEAUMONT HOSPITAL   (Ireland)

Author keywords

familial nephropathy; focal segmental glomerulosclerosis; genetic renal disease; human genetics; molecular genetics

Indexed keywords

ACTIN; INVERTED FORMIN 2; UNCLASSIFIED DRUG;

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; COHORT ANALYSIS; CONTROLLED STUDY; COST EFFECTIVENESS ANALYSIS; EXON; FOCAL GLOMERULOSCLEROSIS; GENE; GENE CLUSTER; GENE FUNCTION; GENETIC REGULATION; GENETIC SCREENING; GENETIC VARIABILITY; HUMAN; INF2 GENE; MAJOR CLINICAL STUDY; MISSENSE MUTATION; OUTCOME ASSESSMENT; PHENOTYPE; PRIORITY JOURNAL;

EID: 83655167305     PISSN: 00852538     EISSN: 15231755     Source Type: Journal    
DOI: 10.1038/ki.2011.297     Document Type: Article

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