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Altered TGFβ signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type I caused by fibulin-4 deficiency

✍ Scribed by Renard, Marjolijn; Holm, Tammy; Veith, Regan; Callewaert, Bert L; Adès, Lesley C; Baspinar, Osman; Pickart, Angela; Dasouki, Majed; Hoyer, Juliane; Rauch, Anita


Book ID
109849390
Publisher
Nature Publishing Group
Year
2010
Tongue
English
Weight
616 KB
Volume
18
Category
Article
ISSN
1018-4813

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