Publication
| Glynn MW, Glover TW, Incomplete processing of mutant lamin A in Hutchinson-Gilford progeria leads to nuclear abnormalities, which are reversed by farnesyltransferase inhibition Human molecular genetics14:2959-69 2005 |
| PubMed ID: 16126733 |
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| Records Return:
(5)
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| Catalog ID | Gender | Age at Sampling | Family | Relationship | Description | Collection_Type_id |
| AG06278 | Male | 38 YR | 1877 | proband | GERONTOLOGY RESEARCH CENTER (GRC) CELL CULTURE COLLECTION | AG |
| AG03513 | Male | 13 YR | 172 | proband | HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | AG |
| AG06297 | Male | 8 YR | | proband | HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | AG |
| GM08398 | Male | 8 YR | | proband | APPARENTLY HEALTHY INDIVIDUAL | GM |
| AG11498 | Male | 14 YR | | proband | HUTCHINSON-GILFORD PROGERIA SYNDROME; HGPS | AG |
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