Search Results - Manabu Wada

  • Showing 1 - 1 results of 1
Refine Results
  1. 1
    Cover Image

    Whole-exome sequencing and digital PCR identified a novel compound heterozygous mutation in the NPHP1 gene in a case of Joubert syndrome and related disorders by Shingo Koyama, Hidenori Sato, Manabu Wada, Toru Kawanami, Mitsuru Emi, Takeo Kato

    Published 2017
    Connect to this object online.
    Book

    Save to List
    Saved in:

Search Tools: