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Mots-clés associés à l'article
Mutated in human diseases
KRT3
EFEMP1
CAPN3
CHEK2
Proteins
CDH23
SDHC
SIPA1
KRT3
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Pubmed
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emedicine
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OMIM
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GLI3
MIM.165240 7p13
Pathology
mutations of
GLI3
in
Greig cephalopoly
syndactyly
syndrome (GCPS) (MIM.175700)
Pallister-Hall syndrome
(PHS) (MIM.146510)
acrocallosal syndrome (MIM.200990)
polydactyly
preaxial polydactyly
type IV (MIM.174700)
postaxial polydactyly
type A1/B (MIM.174200)
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