Fig. 1From: Late diagnosis of Fabry disease caused by a de novo mutation in a patient with end stage renal diseaseMolecular characterization of the c.901 C>T mutation in GLA gene. Sequence analysis of GLA exon 6 in our patient. The top electropherogram is from patient’s mother (a), the lower shows the patient’s mutation (b). The vertical bar indicates the position of the mutationBack to article page