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Mutated in human diseases
ATP2C1
NAT2
SCHAD
JAK3
Proteins
emerin
oxytocin receptor
ERG
SALL1
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emedicine
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SIX3
MIM.603714 2p21
Pathology
germline mutations of
SIX3
in
holoprosencephaly
2 (HPE2) (MIM.157170)
microphtalmia
iris
coloboma
See also
SIXs
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