Novel variants in TNRC6B cause global developmental delay with speech and behavioral abnormalities, short stature, low body weight, café‐au‐lait spots, and metabolic abnormality

Abstract Background TNRC6B deficiency syndrome, also known as global developmental delay with speech and behavioral abnormalities (MIM 619243), is a rare autosomal dominant genetic disease mainly characterized by facial dysmorphism, developmental delay/intellectual disability (DD/ID), speech and lan...

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Váldodahkkit:	Qi Yang, Shan Ou, Xunzhao Zhou, Sheng Yi, Li Lin, Shang Yi, Shujie Zhang, Zailong Qin, Jingsi Luo
Materiálatiipa:	Artigo
Giella:	Inglês
Almmustuhtton:	Wiley 2024-02-01
Ráidu:	Molecular Genetics & Genomic Medicine
Fáttát:	novel de novo variants novel phenotype TNRC6B gene TNRC6B deficiency syndrome
Liŋkkat:	https://doi.org/10.1002/mgg3.2408
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