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Q33558941-34F7455B-7ADF-47F2-80F4-97F7A0BF049B
Q33558941-34F7455B-7ADF-47F2-80F4-97F7A0BF049B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33558941-34F7455B-7ADF-47F2-80F4-97F7A0BF049B
Functional expression of the Wilson disease protein reveals mislocalization and impaired copper-dependent trafficking of the common H1069Q mutation.
P2860
Q33558941-34F7455B-7ADF-47F2-80F4-97F7A0BF049B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33558941-34F7455B-7ADF-47F2-80F4-97F7A0BF049B
rank
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type
BestRank
Statement
wasDerivedFrom
ab8018920b6390aa3b1d032264c43dd27d05d6fa
P2860
Occipital horn syndrome and a mild Menkes phenotype associated with splice site mutations at the MNK locus