Author

L.-j. Wong

Observed names: L J Wong, L.‐J. Wong

Institutions: Baylor College of Medicine, Baylor Genetics

Observed institutions: Baylor College of Medicine, Baylor Genetics

OpenAlex ID: A5113787199

Somatic heterogeneity of the CTG repeat in myotonic dystrophy is age and size dependent.

1995 · L J Wong, T Ashizawa, et al. · Europe PMC (PubMed Central) · 204

FBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndrome

2016 · H. Dai, V.W. Zhang, et al. · Clinical Genetics · 30

POLG-Related Disorders: Muscle Biopsy Findings, Mitochondrial DNA Content and Deletions (P07.206)

2012 · M. Milone, S. Tang, et al. · Neurology · 2

POLG Mutation in a Patient with Cataracts, Early-Onset Distal Muscle Weakness and Atrophy and Ovarian Dysgenesis (P07.207)

2012 · M. R. Bekheirnia, W. Zhang, et al. · Neurology

The Molecular Etiology of Progressive External Ophthalmoplegia (PEO) Associated with Mitochondrial Myopathy (IN7-1.006)

2012 · S. Tang, Y.-W. Huang, et al. · Neurology

Molecular Diagnostic Approaches to Metabolic Myopathies by Target Gene Capture and Next Generation Sequencing (P07.215)

2012 · V. Zhang, H. Cui, et al. · Neurology

The Molecular Etiology of Progressive External Ophthalmoplegia (PEO) Associated with Mitochondrial Myopathy (P07.208)

2012 · S. Tang, Y.-W. Huang, et al. · Neurology

Works count: 7

Citation count: 236

H-index: 2

I10-index: 2