Retinal Dystrophy Due to Paternal Isodisomy for Chromosome 1 or Chromosome 2, with Homoallelism for Mutations in RPE65 or MERTK, Respectively

• Debra A. Thompson

• Christina L. McHenry

• Yun Li

• Julia E. Richards

• Mohammad I. Othman

• Eberhard Schwinger

• Douglas Vollrath

• Samuel G. Jacobson

• Andreas Gal

収録刊行物

• The American Journal of Human Genetics

  The American Journal of Human Genetics 70 (1), 224-229, 2002-01

  Elsevier BV

キーワード

• Genetics (clinical)
• Genetics

詳細情報

• CRID: 1360282588996051712
• NII論文ID: 30017635148
• DOI: 10.1086/338455
• ISSN: 00029297
• Web Site: https://api.elsevier.com/content/article/PII:S0002929707612956?httpAccept=text/xml
• Web Site: https://api.elsevier.com/content/article/PII:S0002929707612956?httpAccept=text/plain
• データソース種別:
  • Crossref
  • CiNii Articles