Figure 2
From: A mutation in the c-Fos gene associated with congenital generalized lipodystrophy
Identification and impact of a homozygous c-fos promoter point mutation in the patient. A) A homozygous point mutation in c-fos promoter (T → A) at position c.-439 was identified in the patient. B) The mutation was not identified in the patient’s father or mother or C) in a restriction based assay with 319 control subjects. Representative samples are shown (lane 1–5; p: patient; M: size standard).