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Mots-clés associés à l'article
Mutated in human diseases
UBR1
LRP7
SNAP29
TMEM16E
Proteins
FGF14
SMOH
PEX7
UBR1
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Pubmed
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emedicine
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OMIM
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RECQL2
MIM.604611 8p12-p11.2
RECQ3, WRN GENE, WRN
germline mutations in Werner symdrome
See also
RECQLs
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