A missense LAMB2 mutation causes congenital nephrotic syndrome by impairing laminin secretion

Journal of the American Society of Nephrology

Volumn 22, Issue 5, 2011, Pages 849-858

  Chen, Ying Maggie ^a   Kikkawa, Yamato ^b   Miner, Jeffrey H ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b TOKYO UNIVERSITY OF PHARMACY AND LIFE SCIENCES   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

LAMININ; LAMININ BETA2; UNCLASSIFIED DRUG;

ARTICLE; CONGENITAL NEPHROTIC SYNDROME; GENE EXPRESSION; GENE LOCATION; GLOMERULUS BASEMENT MEMBRANE; IN VITRO STUDY; KIDNEY FAILURE; MISSENSE MUTATION; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN LOCALIZATION; PROTEINURIA;

EID: 79955640326     PISSN: 10466673     EISSN: 15333450     Source Type: Journal    
DOI: 10.1681/ASN.2010060632     Document Type: Article

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