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Nov 6, 2019 (publication date) through May 18, 2024
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Publication Name
World Journal of Clinical Cases
ISSN
2307-8960
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Li N, Qiao C, Lv Y, Yang T, Liu H, Yu WQ, Liu CX. Compound heterozygous mutation of MUSK causing fetal akinesia deformation sequence syndrome: A case report. World J Clin Cases 2019; 7(21): 3655-3661 [PMID: 31750350 DOI: 10.12998/wjcc.v7.i21.3655] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v7/i21/3655.htm |
| Number | Citing Articles |
| 1 |
Neelam Saini, Vijaya Sree Venkatapuram, Venugopal Satidevi Vineeth, Aditya Kulkarni, Ashwani Tandon, Gayatri Koppolu, Siddaramappa Jagdish Patil, Ashwin Dalal, Shagun Aggarwal. Fetal phenotypes of Mendelian disorders: A descriptive study from India. Prenatal Diagnosis 2022; 42(7): 911 doi: 10.1002/pd.6172
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| 2 |
Benjamin T. Cocanougher, Samuel W. Liu, Ludmila Francescatto, Alexander Behura, Mariele Anneling, David G. Jackson, Kristen L. Deak, Chi D. Hornik, Mai K. ElMallah, Carolyn E. Pizoli, Edward C. Smith, Khoon Ghee Queenie Tan, Marie T. McDonald. The severity of MUSK pathogenic variants is predicted by the protein domain they disrupt. Human Genetics and Genomics Advances 2024; 5(3): 100288 doi: 10.1016/j.xhgg.2024.100288
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