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Mutated in human diseases
RET
TP53
CRYAB
SOX9
Proteins
dystrophin
prestin
SOX9
MKL1
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emedicine
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MVK
MIM.251170 12q24
mevalonate kinase
Pathology
mevalonic aciduria (
MVK
deficiency)
hyper-IgD syndrome
(MIM.260920)
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