Mutations in ARHGEF15 cause autosomal dominant hereditary cerebral small vessel disease and osteoporotic fracture

No abstract is available for this paper.

• Publication year

  2023

• Venue

  Acta Neuropathologica

• Publication date

  2023-03-16

• Fields of study

  Medicine

• Identifiers
  DOI 10.1007/s00401-023-02560-6PMID 36929019
• 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.

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