Nuclear speckleopathies: developmental disorders caused by variants in genes encoding nuclear speckle proteins

No abstract is available for this paper.

• Publication year

  2023

• Venue

  Human Genetics

• Publication date

  2023-03-16

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1007/s00439-023-02540-6PMID 36929417
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Correction: Chen et al. The Chemerin/CMKLR1 Axis Is Involved in the Recruitment of Microglia to Aβ Deposition through p38 MAPK Pathway. Int. J. Mol. Sci. 2022, 23, 9041

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