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Autor:
Karima Djabali, Christina Pedicelli, Dayle McClintock, Mauro Paradisi, Revekka L. Boguslavsky, Howard J. Worman
Publikováno v:
BMC Cell Biology. 6:27
Hutchinson-Gilford progeria syndrome (HGPS, OMIM 176670) is a rare sporadic disorder with an incidence of approximately 1 per 8 million live births. The phenotypic appearance consists of short stature, sculptured nose, alopecia, prominent scalp veins