Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome

Journal of the American Society of Nephrology

Volumn 21, Issue 7, 2010, Pages 1209-1217

  Machuca, Eduardo ^a,b   Benoit, Geneviève ^a,c   Nevo, Fabien ^a   Tête, Marie Josèphe ^a   Gribouval, Olivier ^a   Pawtowski, Audrey ^a   Brandström, Per ^d   Loirat, Chantal ^e,f   Niaudet, Patrick ^a,f   Gubler, Marie Claire ^a   Antignac, Corinne ^a,f  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

^b PONTIFICIA UNIVERSIDAD CATÓLICA DE CHILE   (Chile)

^c UNIVERSITY OF MONTREAL   (Canada)

^d RYHOV COUNTY HOSPITAL   (Sweden)

^e ASSISTANCE PUBLIQUE HÔPITAUX DE PARIS   (France)

^f UNIVERSITÉ PARIS DESCARTES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

NEPHRIN; PODOCIN; WT1 PROTEIN;

ARTICLE; CHILD; CLINICAL FEATURE; CONGENITAL NEPHROTIC SYNDROME; COQ2 GENE; DISEASE COURSE; FAMILIAL DISEASE; FAMILY ASSESSMENT; FEMALE; GENE; GENE DELETION; GENE FUNCTION; GENE MUTATION; GENE SEQUENCE; GENE STRUCTURE; GENOTYPE PHENOTYPE CORRELATION; HISTOLOGY; HUMAN; INFANT; KIDNEY; LAMB2 GENE; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; NEPH1 GENE; NEWBORN; PDSS2 GENE; PLCE1 GENE; PRESCHOOL CHILD; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN DOMAIN; SCREENING;

EID: 77954597034     PISSN: 10466673     EISSN: 15333450     Source Type: Journal    
DOI: 10.1681/ASN.2009121309     Document Type: Article

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