Pages that link to "Q35907284"
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The following pages link to Mutations in CIZ1 cause adult onset primary cervical dystonia (Q35907284):
Displaying 50 items.
- Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesis (Q24602504) (← links)
- Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia (Q24605412) (← links)
- The Role of Cdkn1A-Interacting Zinc Finger Protein 1 (CIZ1) in DNA Replication and Pathophysiology (Q26767281) (← links)
- Genetics in dystonia: an update (Q26866453) (← links)
- Clinical and genetic features of cervical dystonia in a large multicenter cohort (Q27312339) (← links)
- Homozygous mutation of VPS16 gene is responsible for an autosomal recessive adolescent-onset primary dystonia (Q27315952) (← links)
- Role of Gα(olf) in familial and sporadic adult-onset primary dystonia (Q28689107) (← links)
- Tremulous cervical dystonia is likely to be familial: clinical characteristics of a large cohort (Q30592916) (← links)
- Mutations in GNAL: a novel cause of craniocervical dystonia (Q30599478) (← links)
- Genetics of dystonia: what's known? What's new? What's next? (Q33356255) (← links)
- Heterogeneity in primary dystonia: lessons from THAP1, GNAL, and TOR1A in Amish-Mennonites (Q33578955) (← links)
- A headset method for measuring the visual temporal discrimination threshold in cervical dystonia. (Q33935201) (← links)
- Variant Ciz1 is a circulating biomarker for early-stage lung cancer (Q34306595) (← links)
- Genomewide association study in cervical dystonia demonstrates possible association with sodium leak channel (Q34398504) (← links)
- Dystonia--new advances in classification, genetics, pathophysiology and treatment (Q34407916) (← links)
- Primary dystonia: conceptualizing the disorder through a structural brain imaging lens (Q34682292) (← links)
- Dystonia, facial dysmorphism, intellectual disability and breast cancer associated with a chromosome 13q34 duplication and overexpression of TFDP1: case report (Q34815903) (← links)
- Mutations in HPCA cause autosomal-recessive primary isolated dystonia (Q35266327) (← links)
- Inherited isolated dystonia: clinical genetics and gene function. (Q35340179) (← links)
- Dystonia: Five new things. (Q35747957) (← links)
- Recent developments in dystonia (Q35965335) (← links)
- Mutations in GNAL cause primary torsion dystonia (Q36489798) (← links)
- Neuropathology of cervical dystonia (Q36605114) (← links)
- Non-Parkinson movement disorders: Five new things (Q36731540) (← links)
- Association Analysis of NALCN Polymorphisms rs1338041 and rs61973742 in a Chinese Population with Isolated Cervical Dystonia (Q36894132) (← links)
- The genetics of dystonias (Q36934972) (← links)
- Recent advances in the genetics of dystonia (Q36950726) (← links)
- The focal dystonias: current views and challenges for future research (Q37070290) (← links)
- Descriptive epidemiology of cervical dystonia (Q37293573) (← links)
- Next-generation sequencing in understanding complex neurological disease (Q37331388) (← links)
- Pathogenic variants in TUBB4A are not found in primary dystonia (Q37725916) (← links)
- Relationship between DNA replication and the nuclear matrix. (Q38058379) (← links)
- Genetic issues in the diagnosis of dystonias (Q38099832) (← links)
- Primary and secondary dystonic syndromes: an update (Q38113756) (← links)
- The genetics of dystonia: new twists in an old tale (Q38115272) (← links)
- Primary dystonia: moribund or viable (Q38124784) (← links)
- Emerging common molecular pathways for primary dystonia. (Q38124786) (← links)
- Genetics in dystonia (Q38164874) (← links)
- Isolated and combined dystonia syndromes - an update on new genes and their phenotypes (Q38341164) (← links)
- The genetics of the dystonias--a review based on the new classification of the dystonias. (Q38493644) (← links)
- Pain Relief in Cervical Dystonia with Botulinum Toxin Treatment (Q38537633) (← links)
- Hot topic: Recessive mutations in the a3(VI) collagen gene COL6A3 cause early-onset isolated dystonia (Q38564064) (← links)
- Clinical and scientific perspectives on movement disorders: Stanley Fahn's contributions (Q38610367) (← links)
- Genetics of movement disorders in the next-generation sequencing era. (Q38743361) (← links)
- CIZ1 is upregulated in hepatocellular carcinoma and promotes the growth and migration of the cancer cells (Q38823799) (← links)
- CIZ1 promoted the growth and migration of gallbladder cancer cells (Q38937527) (← links)
- Combined occurrence of a novel TOR1A and a THAP1 mutation in primary dystonia (Q38991445) (← links)
- Understanding dystonia: diagnostic issues and how to overcome them (Q39024386) (← links)
- Unmet Needs in Dystonia: Genetics and Molecular Biology-How Many Dystonias? (Q39110426) (← links)
- Using the shared genetics of dystonia and ataxia to unravel their pathogenesis (Q39112358) (← links)