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Comèl-Netherton Syndrome - New Insight Into The Molecular Basis of this Rare Syndrome Characterized by Atopic Diathesis and Immune Deficiency

✍ Scribed by Renner, E.D.; Rylaarsdam, S.; Anover, S.; Hartl, D.; Jayakumar, A.; Belohradsky, B.H.; Ermer, U.; Jin, Y.; Kleiner, G.; Nagel, F.; Zhu, Q.; Claymann, G.L.; Torgerson, T.R.; Ochs, H.D.


Book ID
119278042
Publisher
Elsevier Science
Year
2007
Tongue
English
Weight
59 KB
Volume
119
Category
Article
ISSN
1097-6825

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