A homozygous structural variant of RPGRIP1 is frequently associated with achromatopsia in Japanese patients with IRD

Details 詳細情報について

• CRID

  1360302865544406016

• DOI

  10.1016/j.gimo.2024.101843

• ISSN

  29497744

• Web Site

  https://api.elsevier.com/content/article/PII:S2949774424009890?httpAccept=text/xml

  https://api.elsevier.com/content/article/PII:S2949774424009890?httpAccept=text/plain

• Article Type

  journal article

• Data Source

  • Crossref
  • KAKEN