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Q37115848-4A5906C3-7B1B-4D35-B43D-C926A9E7569B
Q37115848-4A5906C3-7B1B-4D35-B43D-C926A9E7569B
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http://www.wikidata.org/entity/statement/Q37115848-4A5906C3-7B1B-4D35-B43D-C926A9E7569B
SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein
P2860
Q37115848-4A5906C3-7B1B-4D35-B43D-C926A9E7569B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37115848-4A5906C3-7B1B-4D35-B43D-C926A9E7569B
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4c2f0da27d02fa19caa95e5ed3af6287b1750d29
P2860
The SETX missense variation spectrum as evaluated in patients with ALS4-like motor neuron diseases.