Chunmei Lin

700 Fengze Street
Quanzhou, 362000, China

Last Updated: 09/26/2026

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Found 13 publications

Large-scale newborn screening for organic acidemias in Quanzhou, China: a 10-year retrospective observational study.

Large-scale newborn screening for organic acidemias in Quanzhou, China: a 10-year retrospective observational study.

Journal: Scientific reports

Published: January 24, 2025

Newborn screening for primary carnitine deficiency using a second-tier genetic test.

Newborn screening for primary carnitine deficiency using a second-tier genetic test.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: November 16, 2023

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

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

Journal: Heliyon

Published: September 03, 2023

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

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

Journal: Frontiers in pediatrics

Published: September 07, 2021

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

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

Journal: Orphanet journal of rare diseases

Published: April 27, 2021

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

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

Journal: Orphanet journal of rare diseases

Published: January 20, 2021

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

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

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: December 07, 2020

Newborn screening and genetic characteristics of patients with short- and very long-chain acyl-CoA dehydrogenase deficiencies.

Newborn screening and genetic characteristics of patients with short- and very long-chain acyl-CoA dehydrogenase deficiencies.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: June 18, 2020

Newborn screening and variant analysis for methionine adenosyltransferase I/III deficiency

Newborn screening and variant analysis for methionine adenosyltransferase I/III deficiency

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: April 27, 2020

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

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

Journal: BMC pediatrics

Published: April 08, 2020

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

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

Journal: Frontiers in genetics

Published: December 27, 2018

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

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

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: June 24, 2018

Showing 1-12 of 13

Last Updated: 09/26/2026