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Works (4)

Incorporating Next‐Generation Sequencing as a Second‐Tier Test for Primary Carnitine Deficiency

Molecular Genetics & Genomic Medicine
2024-09 | Journal article
DOI: 10.1002/mgg3.70003
Contributors: Yiming Lin; Zhenzhu Zheng; Weihua Lin; Weilin Peng
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Newborn screening for fatty acid oxidation disorders in a southern Chinese population

Heliyon
2024-01 | Journal article
DOI: 10.1016/j.heliyon.2023.e23671
Contributors: Yiming Lin; Chunmei Lin; Bangbang Lin; Zhenzhu Zheng; Weihua Lin; Yanru Chen; Dongmei Chen; Weilin Peng
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Biochemical and molecular features of Chinese patients with glutaric acidemia type 1 detected through newborn screening

Orphanet Journal of Rare Diseases
2021-12 | Journal article
DOI: 10.1186/s13023-021-01964-5
Contributors: Yiming Lin; Wenjun Wang; Chunmei Lin; Zhenzhu Zheng; Qingliu Fu; Weilin Peng; Dongmei Chen
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Glutaric Acidemia type 1 with Atypical Acylcarnitine Profile During Newborn Screening

2021-05-05 | Preprint
DOI: 10.21203/rs.3.rs-474079/v1
Contributors: Yiming Lin; Wenjun Wang; Chunmei Lin; Zhenzhu Zheng; Qingliu Fu; Weilin Peng; Dongmei Chen
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