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

✍ Scribed by Isidor, Bertrand; Lindenbaum, Pierre; Pichon, Olivier; Bézieau, Stéphane; Dina, Christian; Jacquemont, Sébastien; Martin-Coignard, Dominique; Thauvin-Robinet, Christel; Le Merrer, Martine; Mandel, Jean-Louis

Book ID
109914723
Publisher
Nature Publishing Group
Year
2011
Tongue
English
Weight
334 KB
Volume
43
Category
Article
ISSN
1061-4036

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