Copyright
©The Author(s) 2021.
World J Clin Cases. Mar 16, 2021; 9(8): 1853-1862
Published online Mar 16, 2021. doi: 10.12998/wjcc.v9.i8.1853
Published online Mar 16, 2021. doi: 10.12998/wjcc.v9.i8.1853
Figure 3 Sanger sequencing results of the ANKH gene.
ANKH gene test results of the patient, father, mother and his elder brother are shown from top to bottom, respectively: a heterozygous mutation c.1129_1131del on exon 9 of gene ANKH was identified in the patient.
- Citation: Wu JL, Li XL, Chen SM, Lan XP, Chen JJ, Li XY, Wang W. A three-year clinical investigation of a Chinese child with craniometaphyseal dysplasia caused by a mutated ANKH gene. World J Clin Cases 2021; 9(8): 1853-1862
- URL: https://www.wjgnet.com/2307-8960/full/v9/i8/1853.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v9.i8.1853