Fig. 1From: A case report: autosomal recessive Myotonia congenita caused by a novel splice mutation (c.1401 + 1G > A) in CLCN1 gene of a Chinese Han patientPedigree and mutation analysis of the patient. The c.1401 + 1 G > A mutation (red arrow) and c.1657 A > T mutation (red arrow), inherited from his father (I:1) and mother (I:2) respectively, were found in the patient (II)Back to article page