Associated Papers
Novel Compound Heterozygous Variants in the TCTN2 Gene Causing Meckel-Gruber Syndrome 8 in a Non-Consanguineous Chinese Family.
Yang Q et al.
Molecular Genetics & Genomic Medicine, 2025
Tectonic gene mutations in patients with Joubert syndrome.
Huppke P et al.
European Journal of Human Genetics : Ejhg, 2015
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