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Paternal origin of LMNA mutations in Hutchinson–Gilford progeria

✍ Scribed by MR D'Apice; R Tenconi; I Mammi; J van den Ende; G Novelli

Book ID
110723435
Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
68 KB
Volume
65
Category
Article
ISSN
0009-9163

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Hutchinson-Gilford progeria syndrome (HGPS) is a rare premature aging disorder normally caused by a spontaneous heterozygous mutation in the LMNA gene that codes for the nuclear lamina protein lamin A. Several enzymes are involved in the processing of its precursor, prelamin A, to the mature lamin A