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Q33564738-6637865E-C512-44CB-BE68-3A6311BF2D7C
Q33564738-6637865E-C512-44CB-BE68-3A6311BF2D7C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33564738-6637865E-C512-44CB-BE68-3A6311BF2D7C
Chromogranin B P413L variant as risk factor and modifier of disease onset for amyotrophic lateral sclerosis.
P2860
Q33564738-6637865E-C512-44CB-BE68-3A6311BF2D7C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33564738-6637865E-C512-44CB-BE68-3A6311BF2D7C
rank
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wasDerivedFrom
675754b3d7623a25bad0a4fc8eb361b91b58ccc2
P2860
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.