Log in to save to my catalogue

Hyperkinesias in Leigh-like Syndrome with Complex-I Deficiency Due to m.10191TC in MT-ND3

Hyperkinesias in Leigh-like Syndrome with Complex-I Deficiency Due to m.10191TC in MT-ND3

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_gale_infotracmisc_A818772393

Hyperkinesias in Leigh-like Syndrome with Complex-I Deficiency Due to m.10191TC in MT-ND3

About this item

Full title

Hyperkinesias in Leigh-like Syndrome with Complex-I Deficiency Due to m.10191TC in MT-ND3

Publisher

Medknow Publications and Media Pvt. Ltd

Journal title

Annals of African medicine, 2024-07, Vol.23 (3), p.512

Language

English

Formats

Publication information

Publisher

Medknow Publications and Media Pvt. Ltd

Subjects

More information

Scope and Contents

Contents

Hyperkinesias in a patient with complex-I deficiency due to the variant m.10191T>C in MT-ND3 have not been previously reported. The patient is a 32 years-old female with multisystem mitochondrial disease due to variant m.10191T>C in MT-ND3, who has been experiencing episodic, spontaneous or induced abnormal movements since age 23. The abnormal move...

Alternative Titles

Full title

Hyperkinesias in Leigh-like Syndrome with Complex-I Deficiency Due to m.10191TC in MT-ND3

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_gale_infotracmisc_A818772393

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_gale_infotracmisc_A818772393

Other Identifiers

ISSN

1596-3519

DOI

10.4103/aam.aam_32_23

How to access this item