Search - Inserm - Institut national de la santé et de la recherche médicale Access content directly

Filter your results

2 Results
Author: personID (integer) : 892469
Image document

Mutational spectrum and phenotypes in Danish families with hereditary angioedema because of C1 inhibitor deficiency.

Anette Bygum , Christina R. Fagerberg , D. Ponard , Nicole Monnier , Joel Lunardi , et al.
Allergy, 2011, 66 (1), pp.76-84. ⟨10.1111/j.1398-9995.2010.02456.x⟩
Journal articles inserm-00567441v1

Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome

F Buket Ü Basmanav , Laura Cau , Aylar Tafazzoli , Marie-Claire Mechin , Sabrina Wolf , et al.
American Journal of Human Genetics, 2016, 99 (6), pp.1292-1304. ⟨10.1016/j.ajhg.2016.10.004⟩
Journal articles hal-03155007v1