reference/34232764

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/34232764

Outgoing Links

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contentType	Case Reports\|Journal Article
issn	2324-9269
issueIdentifier	8
pageRange	e1998-
publicationName	Molecular Genetics & Genomic Medicine
startingPage	e1998
bibliographicCitation	Giacobbe C, Di Dato F, Palma D, Amitrano M, Iorio R, Fortunato G. Rare variants in PKHD1 associated with Caroli syndrome: Two case reports. Mol Genet Genomic Med. 2022 Aug;10(8):e1998. PMID: 35715958; PMCID: PMC9356553.
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date	2022-06-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC9356553 https://pubmed.ncbi.nlm.nih.gov/35715958 https://doi.org/10.1002/mgg3.1998
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Rare variants in PKHD1 associated with Caroli syndrome: Two case reports
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Total number of triples: 41.