Homozygous deletion, c. 1114-1116del, in exon 8 of the CRPPA gene causes congenital muscular dystrophy in Chinese family: A case report

doi:10.12998/wjcc.v9.i19.5226

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World Journal of Clinical Cases

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2307-8960

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Clin Cases. Jul 6, 2021; 9(19): 5226-5231
Published online Jul 6, 2021. doi: 10.12998/wjcc.v9.i19.5226

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Figure 1 Magnetic resonance imaging of the right calf. The gastrocnemius muscle and soleus muscle showed mild atrophy, mainly in the medial head of the gastrocnemius muscle.

Citation: Yang M, Xing RX. Homozygous deletion, c. 1114-1116del, in exon 8 of the CRPPA gene causes congenital muscular dystrophy in Chinese family: A case report. World J Clin Cases 2021; 9(19): 5226-5231
URL: https://www.wjgnet.com/2307-8960/full/v9/i19/5226.htm
DOI: https://dx.doi.org/10.12998/wjcc.v9.i19.5226