reference/14126545

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/14126545

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publicationName	The American Journal of Human Genetics
startingPage	621
bibliographicCitation	Massink MG, Créton M, Spanevello F, Fennis WM, Cune M, Savelberg SC, Nijman IJ, Maurice M, van den Boogaard MH, van Haaften G. Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia. The American Journal of Human Genetics. 2015 Oct;97(4):621–6. doi: 10.1016/j.ajhg.2015.08.014.
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date	2015-10-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/26387593 https://doi.org/10.1016/j.ajhg.2015.08.014 https://pubmed.ncbi.nlm.nih.gov/PMC4596913
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia
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