✦ LIBER ✦

Absence of integrin α7 causes a novel form of muscular dystrophy

✍ Scribed by Mayer, Ulrike; Saher, Gesine; Fässler, Reinhard; Bornemann, Antje; Echtermeyer, Frank; Mark, Helga von der; Miosge, Nicolai; Pösch, Ernst; Mark, Klaus von der

Book ID: 109918659
Publisher: Nature Publishing Group
Year: 1997
Tongue: English
Weight: 1011 KB
Volume: 17
Category: Article
ISSN: 1061-4036
DOI: 10.1038/ng1197-318

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Integrin α7β1 in Muscular Dystrophy/Myop

Integrin α7β1 in Muscular Dystrophy/Myopathy of Unknown Etiology

✍ Elena Pegoraro; Fulvio Cepollaro; Paola Prandini; Alessandra Marin; Marina Fanin 📂 Article 📅 2002 🏛 American Society for Investigative Pathology 🌐 English ⚖ 858 KB

P.1.20 GOSR2: A novel form of Congenital

P.1.20 GOSR2: A novel form of Congenital Muscular Dystrophy

✍ Tsai, L.; Schwake, M.; Corbett, M.A.; Gecz, J.; Berkovic, S.; Shieh, P.B. 📂 Article 📅 2013 🏛 Elsevier Science 🌐 English ⚖ 47 KB

A benign allelic form of laminin α2 chai

A benign allelic form of laminin α2 chain deficient muscular dystrophy

✍ Yukiko K Hayashi; Tadayuki Ishihara; Kazuhisa Domen; Hisae Hori; Kiichi Arahata 📂 Article 📅 1997 🏛 The Lancet 🌐 English ⚖ 19 KB

A novel mutation in the myotilin gene (M

A novel mutation in the myotilin gene (MYOT) causes a severe form of limb girdle muscular dystrophy 1A (LGMD1A)

✍ Peter Reilich; Sabine Krause; Nicolai Schramm; Ursula Klutzny; Stefanie Bulst; B 📂 Article 📅 2011 🏛 Springer 🌐 English ⚖ 977 KB

Laminin α1 chain mediated reduction of l

Laminin α1 chain mediated reduction of laminin α2 chain deficient muscular dystrophy involves integrin α7β1 and dystroglycan

✍ Kinga I. Gawlik; Ulrike Mayer; Kristina Blomberg; Arnoud Sonnenberg; Peter Ekblo 📂 Article 📅 2006 🏛 Elsevier Science 🌐 English ⚖ 1013 KB

Distinguishing Cardiac Features of a Nov

Distinguishing Cardiac Features of a Novel Form of Congenital Muscular Dystrophy (Salih CMD)

✍ S.A. Subahi 📂 Article 📅 2001 🏛 Springer 🌐 English ⚖ 358 KB