Prenatal Cases Reflect the Complexity of the COL1A1/2 Associated Osteogenesis Imperfecta.
- Published in:
- Genes, 2022, v. 13, n. 9, p. 1578, doi. 10.3390/genes13091578
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- Publication type:
- Article
Works by Sun, Yong-qing
Results: 5
1
2
Identification of novel variations in the NTRK1 gene causing congenital insensitivity to pain with anhidrosis.
- Published in:
- Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 11, p. 1, doi. 10.1002/mgg3.1839
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- Publication type:
- Article
3
Investigation of a Novel NTRK1 Variation Causing Congenital Insensitivity to Pain With Anhidrosis.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.763467
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- Publication type:
- Article
4
Investigation of a Novel LRP6 Variant Causing Autosomal-Dominant Tooth Agenesis.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.688241
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- Publication type:
- Article
5
NTRK1 knockdown induces mouse cognitive impairment and hippocampal neuronal damage through mitophagy suppression via inactivating the AMPK/ULK1/FUNDC1 pathway.
- Published in:
- Cell Death Discovery, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41420-023-01685-7
- By:
- Publication type:
- Article