RecName: Full=Dehydrodolichyl diphosphate synthase complex subunit DHD - Protein

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Phenotype of heterozygous variants of dehydrodolichol diphosphate synthase. [Dev Med Child Neurol. 2022]
Phenotype of heterozygous variants of dehydrodolichol diphosphate synthase.
Jiao X, Xue Y, Yang S, Gong P, Niu Y, Wang Q, Yang H, Xiong H, Zhang Y, Yang Z. Dev Med Child Neurol. 2022 Jan; 64(1):125-134. Epub 2021 Jul 18.
Structural Characterization of Full-Length Human Dehydrodolichyl Diphosphate Synthase Using an Integrative Computational and Experimental Approach. [Biomolecules. 2019]
Structural Characterization of Full-Length Human Dehydrodolichyl Diphosphate Synthase Using an Integrative Computational and Experimental Approach.
Lisnyansky Bar-El M, Lee SY, Ki AY, Kapelushnik N, Loewenstein A, Chung KY, Schneidman-Duhovny D, Giladi M, Newman H, Haitin Y. Biomolecules. 2019 Oct 28; 9(11). Epub 2019 Oct 28.
A case of fatal Type I congenital disorders of glycosylation (CDG I) associated with low dehydrodolichol diphosphate synthase (DHDDS) activity. [Orphanet J Rare Dis. 2016]
A case of fatal Type I congenital disorders of glycosylation (CDG I) associated with low dehydrodolichol diphosphate synthase (DHDDS) activity.
Sabry S, Vuillaumier-Barrot S, Mintet E, Fasseu M, Valayannopoulos V, Héron D, Dorison N, Mignot C, Seta N, Chantret I, et al. Orphanet J Rare Dis. 2016 Jun 24; 11(1):84. Epub 2016 Jun 24.

RefSeq genomic sequence
See the genomic reference sequence for the DHDDS gene (NG_029786.1).
RefSeq protein isoforms
See 35 reference sequence protein isoforms for the DHDDS gene.

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Q86SQ9 [Domain Mapping of Disease Mut...]
Q86SQ9
Domain Mapping of Disease Mutations
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Protein