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  • Mutation in the SLC29A3 Gene in an Egyptian patient with H syndrome: a case report and review of literature

Mutation in the SLC29A3 Gene in an Egyptian patient with H syndrome: a case report and review of literature

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Case Reports HT El-Bassyouni, MM Thomas… - Journal of Pediatric …, 2020 - thieme-connect.com

Chapter : Section16, Section18
Journal Year : 2020
Cited by : 5

Histiocytosis-lymphadenopathy plus syndrome (H syndrome) is caused by mutations in the SLC29A3 gene that result in histiocytic infiltration of numerous organs. Patients suffering from …..... Read More

Keywords : ['h syndrome', 'egyptian patient', 'case report', 'review', 'mutation', 'literature', 'gene']
PubMed Link : https://www.thieme-connect.com/products/ejournals/html/10.1055/s-0039-1697900
Google Scholar Link : https://scholar.google.com/scholar?cites=17155803547657946459&as_sdt=40005&sciodt=0,10&hl=en&num=20