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Jan 26, 2020 (publication date) through Jun 12, 2025
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Publication Name
World Journal of Clinical Cases
ISSN
2307-8960
Publisher of This Article
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Zhang HW, Su BG, Yao Y. OFD1 mutation induced renal failure and polycystic kidney disease in a pair of childhood male twins in China. World J Clin Cases 2020; 8(2): 331-336 [PMID: 32047782 DOI: 10.12998/wjcc.v8.i2.331] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v8/i2/331.htm |
| Number | Citing Articles |
| 1 |
Nunziana Pezzella, Guglielmo Bove, Roberta Tammaro, Brunella Franco. OFD1: One gene, several disorders. American Journal of Medical Genetics Part C: Seminars in Medical Genetics 2022; 190(1): 57 doi: 10.1002/ajmg.c.31962
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| 2 |
Marina Mata, Marina M. Tabbara, Angel Alvarez, Jayanthi Chandar, Marissa Defreitas, Gaetano Ciancio. Case series of kidney transplantation in two pediatric recipients with rare genetic diseases and intellectual disability. BMC Pediatrics 2024; 24(1) doi: 10.1186/s12887-024-05304-x
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