Novel heterozygous GATA3 and SLC34A3 variants in a 6‐year‐old boy with Barakat syndrome and hypercalciuria-Reference-Cited by-同舟云学术

Novel heterozygous GATA3 and SLC34A3 variants in a 6‐year‐old boy with Barakat syndrome and hypercalciuria

Author:

Yu Sha¹²^ORCID,Chen Wen‐xia¹,Lu Wei³,Chen Chao¹,Ni Yihua¹,Duan Bo¹,Wang Bin¹,Wang Huijun²^ORCID,Xu Zheng‐min¹

Affiliation:

1. Department of Otolaryngology‐Head and Neck Surgery Children’s Hospital of Fudan University Shanghai China

2. Center for Molecular Medicine Pediatrics Research Institute Children’s Hospital of Fudan University Shanghai China

3. Endocrinology and Inherited Metabolic Diseases Children’s Hospital of Fudan University Shanghai China

Funder

Science and Technology Commission of Shanghai Municipality

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

Reference28 articles.

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3. Barakat syndrome: clinical polymorphism of the disease;Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics);2023-04-27