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Q28069787-DCA6C762-FB8C-4FBE-908B-E1D6D31883C5
Q28069787-DCA6C762-FB8C-4FBE-908B-E1D6D31883C5
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Statement
http://www.wikidata.org/entity/statement/Q28069787-DCA6C762-FB8C-4FBE-908B-E1D6D31883C5
Expansion, mosaicism and interruption: mechanisms of the CAG repeat mutation in spinocerebellar ataxia type 1
P2860
Q28069787-DCA6C762-FB8C-4FBE-908B-E1D6D31883C5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28069787-DCA6C762-FB8C-4FBE-908B-E1D6D31883C5
rank
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type
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Statement
wasDerivedFrom
8903c95be36f0b05b483aaba36a228ba1d235ad7
P2860
Msh2 deficiency prevents in vivo somatic instability of the CAG repeat in Huntington disease transgenic mice