1. Impaired function of a rare mutation in the MMUT gene causes methylmalonic acidemia in a Chinese patient;Dai;Genet. Res.,2022
2. Prevalence of methylmalonic acidemia among newborns and the clinical-suspected population: a meta-analyse;Jin;J. Maternal-Fetal Neonatal Med.,2022
3. Diversity in the incidence and spectrum of organic acidemias, fatty acid oxidation disorders, and amino acid disorders in Asian countries: Selective screening vs. expanded newborn screening;Shibata;Mol. Genet. Metab. Rep.,2018
4. [Screening for newborn organic aciduria in Zhejiang province:prevalence, outcome and follow-up], Zhejiang da xue xue bao;Hong;J. Zhejiang Univ. Med. Sci.,2017
5. Expanded newborn screening for inborn errors of metabolism by tandem mass spectrometry in Suzhou, China: disease spectrum;Wang;Prevalence, Genetic Charact. Chin. Popul., Front. Genet.,2019