Weilin Peng

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 2

Top Topics

Patient Reported

Ejection Fraction

Top Venues

Molecular genetics & genomic medicine

Orphanet journal of rare diseases

This page only lists publications with an associated author ORCID identifier.

Publications

Yiming Lin, Zhenzhu Zheng, Weihua Lin, Weilin Peng
Incorporating Next-Generation Sequencing as a Second-Tier Test for Primary Carnitine Deficiency. Molecular genetics & genomic medicine 12 (9) (2024)
Yiming Lin, Wenjun Wang, Chunmei Lin, Zhenzhu Zheng, Qingliu Fu, Weilin Peng, Dongmei Chen
Biochemical and molecular features of Chinese patients with glutaric acidemia type 1 detected through newborn screening. Orphanet journal of rare diseases 16 (1) (2021)