Coinheritance of COL4A5 and MYO1E mutations accentuate the severity of kidney disease.

Lennon, Rachel; Stuart, Helen M; Bierzynska, Agnieszka; Randles, Michael J; Kerr, Bronwyn; Hillman, Katherine A; Batra, Gauri; Campbell, Joanna; Storey, Helen; Flinter, Frances A; Koziell, Ania; Welsh, Gavin I; Saleem, Moin A; Webb, Nicholas J A; Woolf, Adrian S

Lennon, Rachel; Stuart, Helen M; Bierzynska, Agnieszka; Randles, Michael J; Kerr, Bronwyn; Hillman, Katherine A; Batra, Gauri; Campbell, Joanna; Storey, Helen; Flinter, Frances A; Koziell, Ania; Welsh, Gavin I; Saleem, Moin A; Webb, Nicholas J A; Woolf, Adrian S.

Affiliation

Lennon R; Wellcome Trust Centre for Cell-Matrix Research, Faculty of Life Sciences, University of Manchester, Michael Smith Building, M13 9PT, Manchester, UK, rachel.lennon@manchester.ac.uk.

Pediatr Nephrol ; 30(9): 1459-65, 2015 Sep.

Article in En | MEDLINE | ID: mdl-25739341

Subject(s)

Collagen Type IV/genetics; Kidney Glomerulus/pathology; Myosin Type I/genetics; Nephritis, Hereditary; Adult; Child; Child, Preschool; Female; Humans; Infant; Inheritance Patterns/genetics; Male; Mutation; Nephritis, Hereditary/diagnosis; Nephritis, Hereditary/genetics; Nephritis, Hereditary/physiopathology; Pedigree; Severity of Illness Index; Siblings

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Myosin Type I / Collagen Type IV / Kidney Glomerulus / Nephritis, Hereditary Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Pediatr Nephrol Journal subject: NEFROLOGIA / PEDIATRIA Year: 2015 Type: Article

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