reference/35948418

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/35948418

Outgoing Links

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endingPage	439
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bibliographicCitation	De Ridder W, de Vries G, Van Schil K, Deconinck T, Mouly V, Straub V, Baets J. A homozygous loss of function variant in POPDC3: From invalidating exercise intolerance to a limb-girdle muscular dystrophy phenotype. Neuromuscul Disord. 2023 May;33(5):432–9. doi: 10.1016/j.nmd.2023.04.003. PMID: 37104941.
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date	202305
identifier	https://doi.org/10.1016/j.nmd.2023.04.003 https://pubmed.ncbi.nlm.nih.gov/37104941
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	A homozygous loss of function variant in POPDC3: From invalidating exercise intolerance to a limb-girdle muscular dystrophy phenotype
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