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Mutated in human diseases
AHI1
FOXE3
SQSTM1
FGFR1
Proteins
PEX10
UCP2
CBFB
AHI1
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emedicine
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PITX3
MIM.602669 10q25
Pathology
congenital
cataract
anterior segment mesenchymal dysgenesis (ASMD) (MIM.107250)
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