Clinical diagnostic exome sequencing in dystonia: Genetic testing challenges for complex conditions-Reference-Cited by-同舟云学术

Clinical diagnostic exome sequencing in dystonia: Genetic testing challenges for complex conditions

Published:2019-10-30 Issue:2 Volume:97 Page:305-311
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Powis Zöe¹^ORCID,Towne Meghan C.¹^ORCID,Hagman Kelly D.F.²^ORCID,Blanco Kirsten¹,Palmaer Erika²^ORCID,Castro Andrew³,Sajan Samin A.²,Radtke Kelly²,Feyma Timothy J.⁴,Juliette Kali⁴,Tang Sha²,Sidiropoulos Christos⁵

Affiliation:

1. Department of Clinical Research AffairsAmbry Genetics Aliso Viejo California

2. Department of Clinical GenomicsAmbry Genetics Aliso Viejo California

3. Department of Genetic SpecialistsAmbry Genetics Aliso Viejo California

4. Department of NeurologyGillette Children's Specialty Healthcare St Paul Minnesota

5. Department of Neurology and OphthalmologyMichigan State University East Lansing Michigan

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.13657

Reference21 articles.

1. Phenomenology and classification of dystonia: A consensus update

2. Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force

3. The impact and prognosis for dystonia in childhood including dystonic cerebral palsy: a clinical and demographic tertiary cohort study

4. Update on the Genetics of Dystonia

5. Diagnosis and Treatment of Dystonia

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