Chunmei Lin

发表

Biochemical and molecular features of Chinese patients with glutaric acidemia type 1 detected through newborn screening

Yiming Lin, Wenjun Wang, Chunmei Lin, 2021, Orphanet Journal of Rare Diseases.

Glutaric Acidemia type 1 with Atypical Acylcarnitine Profile During Newborn Screening

Yiming Lin, Wenjun Wang, Chunmei Lin, 2021 .

Increased primary carnitine deficiency detection through second-tier newborn genetic screening

Yiming Lin, Chunmei Lin, Qingliu Fu, 2021 .

Increased detection of primary carnitine deficiency through second-tier newborn genetic screening

Yiming Lin, Chunmei Lin, Qingliu Fu, 2021, Orphanet Journal of Rare Diseases.

Combined primary carnitine deficiency with neonatal intrahepatic cholestasis caused by citrin deficiency in a Chinese newborn

Yiming Lin, Chunmei Lin, Zhenzhu Zheng, 2020, BMC Pediatrics.

Three Novel and One Potential Hotspot CPT1A Variants in Chinese Patients With Carnitine Palmitoyltransferase 1A Deficiency

Yiming Lin, Chunmei Lin, Qingliu Fu, 2021, Frontiers in Pediatrics.

Mild clinical features of isolated methylmalonic acidemia associated with a novel variant in the MMAA gene in two Chinese siblings

Yiming Lin, Chunmei Lin, Zhenzhu Zheng, 2018, BMC medical genetics.

Newborn screening and molecular features of patients with multiple acyl-CoA dehydrogenase deficiency in Quanzhou, China

Yiming Lin, Chunmei Lin, Qingliu Fu, 2021, Journal of pediatric endocrinology & metabolism : JPEM.

Biochemical, Clinical, and Genetic Characteristics of Short/Branched Chain Acyl-CoA Dehydrogenase Deficiency in Chinese Patients by Newborn Screening

Hongzhi Gao, Yiming Lin, Chunmei Lin, 2019, Front. Genet..

Clinical, biochemical and genetic analysis of Chinese patients with isobutyryl-CoA dehydrogenase deficiency.

Yiming Lin, Chunmei Lin, Zhenzhu Zheng, 2018, Clinica chimica acta; international journal of clinical chemistry.

Newborn screening for fatty acid oxidation disorders in a southern Chinese population

Yiming Lin, Chunmei Lin, Zhenzhu Zheng, 2023, Heliyon.