-
2122697
CCM1
cerebral cavernous malformation type 1
7
-
2122707
CCM1
Causative loss-of-function mutations have been identified in three genes, KRIT1
2
-
2122708
CCM1
CCMs; KRIT1
2
-
2122712
CCM1
cascades resulting from deficiencies in KRIT1
1
-
2122700
CCM1
causative loci on chromosomes 7q21.2
1
-
2122701
CCM1
cavernous cerebral malformations type 1
1
-
2122704
CCM1
CCM genes are identified as Krit 1
1
-
2122705
CCM1
CCM is caused by mutations in KRIT1
1
-
2122702
CCM1
CCM is typically associated with mutations in KRIT1
1
-
2122703
CCM1
CCM loci have been identified, on chromosomes 7q21-22
1
-
2122711
CCM1
CCM type 1
1
-
2122709
CCM1
CCMs are linked to loss-of-function mutations in KRIT1
1
-
2122710
CCM1
CCMs has identified three different loci at 7q21.2
1
-
2122706
CCM1
CEACAM1 N-terminal Ig-like domain
1
-
2122699
CCM1
cerebral capillary malformation gene-1
1
-
2122698
CCM1
cerebral CM1
1
-
2122696
CCM1
clinic after genetic testing identified a familial KRIT1
1