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Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: A novel mutation of HOXA11 in a patient with septate uterus

Fig. 1

A novel variation of HOX11 identified in a patient with septate uterus. a Electropherograms obtained by direct sequencing of PCR products showing the heterozygous G to A substitution at nucleotide 763 of HOXA11 gene in the patient and the patient’s mother, but not in a control subject or in the patient’s father. b The p.E255K mutation situated in the homeodomain of HOXA11. c Sequence alignment of HOXA11 protein among different species showing the mutation located in the highly conserved site of the protein

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