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Truncating mutations in the last exon of NOTCH2 cause a rare skeletal disorder with osteoporosis

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Description scientific article
Author/s

author: Jean-Louis Mandel  Pierre Lindenbaum  Martine Le Merrer  Christian Dina  Cédric Le Caignec  Dominique Martin-Coignard  Stéphane Bézieau  Valérie Cormier-Daire  Laurence Faivre  Richard Redon  Christel Thauvin-Robinet 

Publication date April 2011
Language English
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