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World J Gastroenterol. Jan 7, 2014; 20(1): 326-329
Published online Jan 7, 2014. doi: 10.3748/wjg.v20.i1.326
Published online Jan 7, 2014. doi: 10.3748/wjg.v20.i1.326
Figure 1 Pedigree of the patient shown with genomic DNA sequences in exons 14 and 20 of the VPS33B gene in the patient and her parents.
The arrow in exon 14 identifies c.1033delA in the patient and her mother. The arrow in exon 20 identifies c.1567C>T in the patient and her father.
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Citation: Li LT, Zhao J, Chen R, Wang JS. Two novel
VPS33B mutations in a patient with arthrogryposis, renal dysfunction and cholestasis syndrome in mainland China. World J Gastroenterol 2014; 20(1): 326-329 - URL: https://www.wjgnet.com/1007-9327/full/v20/i1/326.htm
- DOI: https://dx.doi.org/10.3748/wjg.v20.i1.326