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Mots-clés associés à l'article
Mutated in human diseases
FH
DKC1
PTEN
CLDN1
Proteins
TLN1
DSG4
paraoxonase
FH
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Pubmed
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emedicine
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OMIM
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NORD
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KRT13
MIM.148065 17q21-q22
keratin-13, cytokeratin-13
Pathology
germline mutation in white sponge nevus (MIM.193900)
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