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Q40301932-F1D2AD41-867A-4AB4-87B3-40AC4FFAC631
Q40301932-F1D2AD41-867A-4AB4-87B3-40AC4FFAC631
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Statement
http://www.wikidata.org/entity/statement/Q40301932-F1D2AD41-867A-4AB4-87B3-40AC4FFAC631
Asymptomatic isolated human glycerol kinase deficiency associated with splice-site mutations and nonsense-mediated decay of mutant RNA.
P2860
Q40301932-F1D2AD41-867A-4AB4-87B3-40AC4FFAC631
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40301932-F1D2AD41-867A-4AB4-87B3-40AC4FFAC631
rank
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wasDerivedFrom
b528947f7dad87c90d5d47016aa67d5688d50302
P2860
Phenotypes of patients with "simple" Mendelian disorders are complex traits: thresholds, modifiers, and systems dynamics.