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SCARB2
LE WE PMID CA
SCARB212162SCARB2

Action Myoclonus Renal Failure Syndrome

ACTN4 Alpha actinin4

CD151 Tetraspanin

CD2AP

Coenzyme Q10

Congenital nephrotic syndrome finnish type

COQ2

Denys Drash syndrome

Early onset familial nephrotic syndrome

Epstein s syndrome

Fechtner s syndrome

Frasier s syndrome

Galloway Mowat s syndrome

GMS1

Kidney (FSGS)

LAMB2 Laminin beta2

Laminin

LMNA Lamin C Prelamin A

LMX1B

Mandibuloacral dysplasia

May Hegglin anomaly

MYH9

Nail patella syndrome

NPHS1 Nephrin

NPHS2

Phospholipase C epsilon

Pierson s syndrome

PLCE1

Podocin

SCARB2

Schimke immunoosseous dysplasia

Sebastian s syndrome

SMARCALI

Steroid resistant nephrotic syndrome SRN1

TRPC6

WT1

ZMPSTE24

2009  
1
Molecular genetic analysis of podocyte genes in focal segmental glomerulosclerosis--a review.
[19562370] Eur J Pediatr 168(11): 1291-304 (2009)

Downloaded from http://www.kidney.de - The Database of Free Medical Reviews - The Metatextbook of Medicine - Ossip Groth

All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.


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