Results
|
401.
|
|
|
402.
|
|
|
403.
|
|
|
404.
|
|
|
405.
|
Electromyographic Features in a Chinese Cohort With Hereditary Skeletal Muscle Channelopathies. [electronic resource] by
- Sun, Jian
- Luo, Sushan
- Song, Jie
- Huang, Jun
- Cai, Shuang
- Zhu, Wenhua
- Zhou, Lei
- Xi, Jianying
- Lin, Jie
- Lu, Jiahong
- Xu, Minjie
- Dou, Tonghai
- Zhao, Chongbo
- Qiao, Kai
Producer: 20200921
In:
Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society vol. 37
Availability: No items available.
|
|
406.
|
|
|
407.
|
|
|
408.
|
Follistatin in chondrocytes: the link between TRPV4 channelopathies and skeletal malformations. [electronic resource] by
- Leddy, Holly A
- McNulty, Amy L
- Lee, Suk Hee
- Rothfusz, Nicole E
- Gloss, Bernd
- Kirby, Margaret L
- Hutson, Mary R
- Cohn, Daniel H
- Guilak, Farshid
- Liedtke, Wolfgang
Producer: 20141006
In:
FASEB journal : official publication of the Federation of American Societies for Experimental Biology vol. 28
Availability: No items available.
|
|
409.
|
|
|
410.
|
|
|
411.
|
|
|
412.
|
|
|
413.
|
|
|
414.
|
Penetrance and expressivity of the R858H CACNA1C variant in a five-generation pedigree segregating an arrhythmogenic channelopathy. [electronic resource] by
- Gardner, R J McKinlay
- Crozier, Ian G
- Binfield, Alex L
- Love, Donald R
- Lehnert, Klaus
- Gibson, Kate
- Lintott, Caroline J
- Snell, Russell G
- Jacobsen, Jessie C
- Jones, Peter P
- Waddell-Smith, Kathryn E
- Kennedy, Martin A
- Skinner, Jonathan R
Producer: 20190315
In:
Molecular genetics & genomic medicine vol. 7
Availability: No items available.
|
|
415.
|
|
|
416.
|
|
|
417.
|
|
|
418.
|
|
|
419.
|
|
|
420.
|
|