Results
|
|
41.
|
|
|
|
42.
|
|
|
|
43.
|
|
|
|
44.
|
|
|
|
45.
|
|
|
|
46.
|
|
|
|
47.
|
|
|
|
48.
|
|
|
|
49.
|
|
|
|
50.
|
|
|
|
51.
|
|
|
|
52.
|
|
|
|
53.
|
Congenital muscular dystrophy, myasthenic symptoms and epidermolysis bullosa simplex (EBS) associated with mutations in the PLEC1 gene encoding plectin. [electronic resource] by
- Forrest, Katharine
- Mellerio, Jemima E
- Robb, Stephanie
- Dopping-Hepenstal, Patricia J C
- McGrath, John A
- Liu, Lu
- Buk, Stefan J A
- Al-Sarraj, Safa
- Wraige, Elizabeth
- Jungbluth, Heinz
Producer: 20110121
In:
Neuromuscular disorders : NMD vol. 20
Availability: No items available.
|
|
|
54.
|
|
|
|
55.
|
|
|
|
56.
|
|
|
|
57.
|
|
|
|
58.
|
|
|
|
59.
|
|
|
|
60.
|
|