reference/35138077

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/35138077

Outgoing Links

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contentType	Journal Article\|Research Support, Non-U.S. Gov't
endingPage	705
issn	0001-6322 1432-0533
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pageRange	681-705
publicationName	Acta Neuropathologica
startingPage	681
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bibliographicCitation	Ding X, Chen Y, Guo C, Fu Y, Qin C, Zhu Q, Wang J, Zhang R, Tian H, Feng R, Liu H, Liang D, Wang G, Teng J, Li J, Tang B, Wang X. Mutations in ARHGEF15 cause autosomal dominant hereditary cerebral small vessel disease and osteoporotic fracture. Acta Neuropathol. 2023 May;145(5):681–705. doi: 10.1007/s00401-023-02560-6. PMID: 36929019.
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date	2023-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/36929019 https://doi.org/10.1007/s00401-023-02560-6
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Mutations in ARHGEF15 cause autosomal dominant hereditary cerebral small vessel disease and osteoporotic fracture
discusses	http://id.nlm.nih.gov/mesh/M000764561
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Incoming Links

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Total number of triples: 54.