ETM2 (gene): Difference between revisions
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'''ETM2''' is a [[gene]] associated with [[essential tremor]].<ref> |
'''ETM2''' is a [[gene]] associated with [[essential tremor]].<ref>{{Cite journal | doi=10.1002/ajmg.a.31958| pmid=18203159|title = Heritable essential tremor-idiopathic normal pressure hydrocephalus (ETINPH)| journal=American Journal of Medical Genetics Part A| volume=146A| issue=4| pages=433–439|year = 2008|last1 = Zhang|first1 = Jun| last2=Williams| first2=Michael A.| last3=Rigamonti| first3=Daniele}}</ref> |
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==References== |
==References== |
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Revision as of 16:25, 22 January 2019
| essential tremor 2 | |
|---|---|
| Identifiers | |
| Symbol | ETM2 |
| NCBI gene | 2112 |
| HGNC | 3487 |
| OMIM | 602134 |
| Other data | |
| Locus | Chr. 2 p25-2p22 |
ETM2 is a gene associated with essential tremor.[1]
References
- ^ Zhang, Jun; Williams, Michael A.; Rigamonti, Daniele (2008). "Heritable essential tremor-idiopathic normal pressure hydrocephalus (ETINPH)". American Journal of Medical Genetics Part A. 146A (4): 433–439. doi:10.1002/ajmg.a.31958. PMID 18203159.
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