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contentType Journal Article|Research Support, Non-U.S. Gov't
issn 1750-1172
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publicationName Orphanet Journal of Rare Diseases
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bibliographicCitation Phetthong T, Tim-Aroon T, Khongkraparn A, Noojarern S, Kuptanon C, Wichajarn K, Sathienkijkanchai A, Suphapeetiporn K, Charoenkwan P, Tantiworawit A, Noentong N, Wattanasirichaigoon D. Gaucher disease: clinical phenotypes and refining GBA mutational spectrum in Thai patients. Orphanet Journal of Rare Diseases. 2021 Dec 20;16(1):519. doi: 10.1186/s13023-021-02151-2.
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date 2021-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://pubmed.ncbi.nlm.nih.gov/PMC8686639
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language English
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title Gaucher disease: clinical phenotypes and refining GBA mutational spectrum in Thai patients
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Total number of triples: 38.