Fig. 1From: A rare c.183_187dupCTCAC mutation of the acetylcholine receptor CHRNE gene in a South Asian female with congenital myasthenic syndrome: a case reporta Family tree of patient. Her paternal grandfather had died of malignancy. Arrow indicates proband. b Sequencing traces from a region within exon 2 of the CHRNE gene from a healthy individual and the patient. The 5-nucleotide insertion c.127insCTCAC is indicatedBack to article page