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#610651 - XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B; XPB
XERODERMA PIGMENTOSUM B/COCKAYNE SYNDROME, INCLUDED
Cytogenetic locations: 12005975
Gene summaries Genetic tests Medical literature
*133510 - ERCC EXCISION REPAIR 3, TFIIH CORE COMPLEX HELICASE SUBUNIT; ERCC3
Cytogenetic locations: 16537383
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