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World J Clin Cases. Mar 16, 2014; 2(3): 67-71
Published online Mar 16, 2014. doi: 10.12998/wjcc.v2.i3.67
Published online Mar 16, 2014. doi: 10.12998/wjcc.v2.i3.67
Figure 4 Detection of the LMNA mutation in the Hutchinson-Gilford progeria syndrome patient.
Shown here are portions of the DNA-sequence electropherogram of the LMNA exon 11 of the affected patient, his parents and older sister. Compared to the normal sequence, the affected patient has a heterozygous C-to-T substitution at nucleotide position 1824 in the LMNA gene, which does not change the amino acid (G608G).
- Citation: Alves DB, Silva JM, Menezes TO, Cavaleiro RS, Tuji FM, Lopes MA, Zaia AA, Coletta RD. Clinical and radiographic features of Hutchinson-Gilford progeria syndrome: A case report. World J Clin Cases 2014; 2(3): 67-71
- URL: https://www.wjgnet.com/2307-8960/full/v2/i3/67.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v2.i3.67