HOXA11 is another monogenic cause of congenital anomalies of the kidney and urinary tract
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology,Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00467-022-05756-2.pdf
Reference3 articles.
1. Kagan M, Pleniceanu O, Vivante A (2022) The genetic basis of congenital anomalies of the kidney and urinary tract. Pediatr Nephrol 37:2231–2243
2. Saygili S, Atayar E, Canpolat N, Elicevik M, Kurugoglu S, Sever L, Caliskan S, Ozaltin F (2020) A homozygous HOXA11 variation as a potential novel cause of autosomal recessive congenital anomalies of the kidney and urinary tract. Clin Genet 98:390–395
3. Sezer A, Percin FE, Kazan HH, Kayhan G, Akturk M (2022) A de novo heterozygous HOXA11 variant in a patient with mesomelic dysplasia with urogenital abnormalities. Am J Med Genet A 188:1890–1895
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1. HOXA11 is another monogenic cause of congenital anomalies of the kidney and urinary tract—Reply;Pediatric Nephrology;2022-11-19
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