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Year | Number of Results |
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2013 | 1 |
2017 | 1 |
2024 | 0 |
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Transient compartment-like syndrome and normokalaemic periodic paralysis due to a Ca(v)1.1 mutation.
Brain. 2013 Dec;136(Pt 12):3775-86. doi: 10.1093/brain/awt300. Epub 2013 Nov 15.
Brain. 2013.
PMID: 24240197
Free PMC article.
De novo Mutation in CACNA1S Gene in a 20-Year-Old Man Diagnosed with Metabolic Myopathy.
Edizadeh M, Vazehan R, Javadi F, Dehdahsi S, Fadaee M, Faraji Zonooz M, Parsimehr E, Ahangari F, Abolhassani A, Kalhor Z, Fattahi Z, Beheshtian M, Kariminejad A, Akbari MR, Najmabadi H, Nafissi S.
Edizadeh M, et al.
Arch Iran Med. 2017 Sep;20(9):617-620.
Arch Iran Med. 2017.
PMID: 29048924
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