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1
Q45070374-56B43CAE-13D3-48A7-A39F-B8EE9FC2E3E2
Q45070374-56B43CAE-13D3-48A7-A39F-B8EE9FC2E3E2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q45070374-56B43CAE-13D3-48A7-A39F-B8EE9FC2E3E2
A novel inborn error of the coenzyme Q10 biosynthesis pathway: cerebellar ataxia and static encephalomyopathy due to COQ5 C-methyltransferase deficiency.
P2860
Q45070374-56B43CAE-13D3-48A7-A39F-B8EE9FC2E3E2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q45070374-56B43CAE-13D3-48A7-A39F-B8EE9FC2E3E2
rank
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type
BestRank
Statement
wasDerivedFrom
c32a66ba7fa38300e218f764c31077746e8ae283
P2860
Molecular analysis of the Retinoic Acid Induced 1 gene (RAI1) in patients with suspected Smith-Magenis syndrome without the 17p11.2 deletion.