International Clinical Trial: MT-ND3 Gene m.10197G>A Variant Leads to Leigh Syndrome in a Pedigree and Literature Review

Geneva, Aug. 6 -- International Clinical Trials Registry received information related to the study (ChiCTR2600129043) titled 'MT-ND3 Gene m.10197G>A Variant Leads to Leigh Syndrome in a Pedigree and Literature Review' on July 29.

Study Type: Observational study

Study Design: Case study

Primary Sponsor: Shenzhen Second People's Hospital

Condition: MT-ND3 Gene m.10197G>A Variant Leads to Leigh Syndrome

Recruitment Status: Not Recruiting

Phase: N/A

Date of First Enrollment: 2025-12-01

Target Sample Size: Single-family pedigree:2;

Countries of Recruitment: China

To know more, visit https://www.chictr.org.cn/showproj.html?proj=311824

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