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

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

193

Citations

12

References

2011

Year

Bertrand Isidor, Pierre Lindenbaum, Olivier Pichon, Stéphane Bezieau, Christian Dina, Sébastien Jacquemont, Dominique Martin‐Coignard, Christel Thauvin‐Robinet, Martine Le Merrer, Jean‐Louis Mandel,

Nature Genetics

Bone DiseaseLast ExonRare Skeletal DisorderMendelian DisorderBone Morphogenic ProteinGenetic DisorderGeneticsPathologyOsteoporosisMedicineOrthopaedic Surgery

References

	Year	Citations

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