Kategorie:
PubID
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MIM
ACTN4
ANLN
APOL1
ARHGAP24
ARHGDIA
AVIL
CD2AP
23165304 Alport syndrome--insights from basic and clinical research
COL4A3
23165304 Alport syndrome--insights from basic and clinical research
COL4A4
23165304 Alport syndrome--insights from basic and clinical research
COL4A5
COQ2
COQ6
COQ8B
CRB2
CUBN
DGKE
DLC1
EMP2
FAT1
FN1
INF2
ITGA3
ITGB4
ITSN1
KANK1
KANK2
KANK4
LAMB2
LMX1B
LRP2
MAGI2
MT-TL1
25077172 Mutation spectrum and genotype-phenotype correlations in a large French cohort of MYH9-Related Disorders
MYH9
MYO1E
NPHS1
NPHS2
NUP107
NUP205
NUP93
PAX2
PDSS2
PLCE1
PTPRO
SCARB2
SGPL1
SMARCAL1
TNS2
TRPC6
TTC21B
WDR73
WT1
XPO5