Alport syndrome with diffuse leiomyomatosis

American Journal of Medical Genetics

Volumn 119 A, Issue 3, 2003, Pages 381-385

  Anker, Martina C ^a   Arnemann, Joachim ^a   Neumann, Katrin ^a   Ahrens, Peter ^a   Schmidt, Helga ^a   König, Rainer ^a  

^a UNIVERSITY HOSPITAL FRANKFURT   (Germany)

Author keywords

Alport syndrome; Collagen 4 alpha 5 collagen 4 alpha 6; Leiomyomatosis; Microdeletion; Nephropathy; Sensorineural hearing loss; X linked

Indexed keywords

BARIUM; DNA;

ALPORT SYNDROME; ARTICLE; CASE REPORT; CHILD; CONGENITAL CATARACT; DISEASE ASSOCIATION; ELECTRON MICROSCOPY; ESOPHAGUS BIOPSY; GENE DELETION; GENE MUTATION; HEMATURIA; HUMAN; KIDNEY BIOPSY; KIDNEY DISEASE; KIDNEY FAILURE; LEIOMYOMATOSIS; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PERCEPTION DEAFNESS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; THORAX RADIOGRAPHY;

EID: 0042322471     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.20019     Document Type: Article

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