Publication
| Weeda G, van Ham RC, Vermeulen W, Bootsma D, van der Eb AJ, Hoeijmakers JH, A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome. Cell62:777-91 1990 |
| PubMed ID: 2167179 |
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| Records Return:
(3)
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| Catalog ID | Gender | Age at Sampling | Family | Relationship | Description | Collection_Type_id |
| GM01855 | Female | 64 YR | 283 | mother | XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B; XPB | GM |
| GM02252 | Female | 31 YR | 283 | proband | XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B; XPB | GM |
| GM11394 | Male | 82 YR | 283 | father | XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B; XPB | GM |
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