Showing 1 - 1 results of 1 for search 'Sheng‐Jia Lin (18877600)', query time: 0.01s Refine Results
  1. 1
    Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function

    Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function by Sheng‐Jia Lin (18877600)

    Published 2022
    Save to List
    Saved in:

Search Tools: