Deyun Lu

The Follow-Up of Chinese Patients in cblC Type Methylmalonic Acidemia Identified Through Expanded Newborn Screening

Shiying Ling, Shengnan Wu, Ruixue Shuai et al. · Frontiers in Genetics · 2022 · 29 citations · Full text

Medicine, Genetics, Pediatrics +17

Clinical and molecular characteristics of 69 Chinese patients with ornithine transcarbamylase deficiency

Deyun Lu, Feng Han, Wenjuan Qiu et al. · Orphanet Journal of Rare Diseases · 2020 · 26 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Different mutations in the <i>MMUT</i> gene are associated with the effect of vitamin B12 in a cohort of 266 Chinese patients with mut‐type methylmalonic acidemia: A retrospective study

Yue Yu, Ruixue Shuai, Lili Liang et al. · Molecular Genetics & Genomic Medicine · 2021 · 22 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Newborn screening of maple syrup urine disease and the effect of early diagnosis

Ting Chen, Deyun Lu, Feng Xu et al. · Clinica Chimica Acta · 2023 · 21 citations

Medicine, Pediatrics, Preventive Medicine +11

A rare mutation c.1663G &gt; A (p.A555T) in the MMUT gene associated with mild clinical and biochemical phenotypes of methylmalonic acidemia in 30 Chinese patients

Lili Liang, Ruixue Shuai, Yue Yu et al. · Orphanet Journal of Rare Diseases · 2021 · 15 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16