✦ LIBER ✦

G.P.7.03 Mutations in TPM2 and TPM3 causing nemaline myopathy or arthrogryposis

✍ Scribed by V.L. Lehtokari; H. Kalimo; K. Pelin; C. Wallgren-Pettersson

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

C.P.1.13 A homozygous null mutation in T

✍ P. Jouk; A. Labarre-Vila; P. Mezin; S. Drouhin; I. Marty; J. Lunardi; N. Monnier 📂 Article 📅 2007 🏛 Elsevier Science 🌐 English ⚖ 64 KB

Force-Sarcomere Length Relations in Pati

✍ de Winter, Josine M.; Joureau, Barbara; Ottenheijm, Coen A.C. 📂 Article 📅 2014 🏛 Biophysical Society 🌐 English ⚖ 47 KB

C.P.15 K7del is a recurrent TPM2 nemalin

✍ Mokbel, N.; Ilkovski, B.; Memo, M.; Marttila, M.; Kreissl, M.; Wallgren-Petterss 📂 Article 📅 2012 🏛 Elsevier Science 🌐 English ⚖ 53 KB

P.9.6 Combined cap disease and nemaline

✍ Malfatti, E.; Schaeffer, U.; Chapon, F.; Yang, Y.; Eymard, B.; Xu, R.; Laporte, 📂 Article 📅 2013 🏛 Elsevier Science 🌐 English ⚖ 46 KB

C.P.16 Mutations in the β-tropomyosin (T

✍ Marttila, M.; Lehtokari, V.-L.; Wallgren-Pettersson, C. 📂 Article 📅 2012 🏛 Elsevier Science 🌐 English ⚖ 64 KB