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Object |
| contentType |
Case Reports|Journal Article|Research Support, Non-U.S. Gov't |
| issn |
1099-498X
1521-2254 |
| issueIdentifier |
6 |
| pageRange |
e3335- |
| publicationName |
The Journal of Gene Medicine |
| startingPage |
e3335 |
| bibliographicCitation |
Zhang X, Gu Y, Fu W. A novel PPRC1 point mutation in a Chinese family with premature ovarian failure: A case study. The Journal of Gene Medicine. 2021 Apr 19;23(6). doi: 10.1002/jgm.3335. |
| creator |
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http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-8307-5176
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_76fc6e5d68fadbe0406a49c4b616918a |
| date |
2021-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| identifier |
https://doi.org/10.1002/jgm.3335
https://pubmed.ncbi.nlm.nih.gov/33818872 |
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http://rdf.ncbi.nlm.nih.gov/pubchem/journal/21672
https://portal.issn.org/resource/ISSN/1099-498X
https://portal.issn.org/resource/ISSN/1521-2254 |
| language |
English |
| source |
https://pubmed.ncbi.nlm.nih.gov/
https://www.crossref.org/ |
| title |
A novel PPRC1 point mutation in a Chinese family with premature ovarian failure: A case study |
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