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Paper Details

Association of Rare CYP39A1 Variants With Exfoliation Syndrome Involving the Anterior Chamber of the Eye.
JAMA
12
2021
CYP39A1, CYP39A1 Variants, CYP39A1 alleles, CYP39A1 damaging alleles, CYP39A1 sequence variants, CYP39A1 transcript, CYP39A1 variants, Exfoliation Syndrome, Exfoliation syndrome, Participants, ciliary body tissues, coding-sequence genetic variants, exfoliation syndrome, glaucoma, irreversible blindness, participants, persons, systemic disorder, wild-type CYP39A1, women
Author NameAffiliation
Satoshi IshikoDepartment of Medicine and Engineering Combined Research Institute, Asahikawa Medical University
Akitoshi YoshidaAsahikawa Medical University
Federico Martin??n-TorresHospital Clinico Universitario de Santiago and GENVIP Research Group, Instituto de Investigacion Sanitaria, University of Santiago de Compostela
Antonio SalasUnidade de Xenetica, Instituto de Ciencias Forenses, Universidade de Santiago de Compostela, Instituto de Investigacion Sanitaria, Hospital Clinico Universitario de Santiago
Anand SwaroopUniversitatsklinikum Erlangen, Friedrich-Alexander-Universitat Erlangen-Nurnberg
Jessica N Cooke BaileyInstitute for Computational Biology, Case Western Reserve University School of Medicine
Jonathan L HainesInstitute for Computational Biology, Case Western Reserve University School of Medicine
Jonathan L HainesInstitute for Computational Biology, Case Western Reserve University School of Medicine
Louis R PasqualeIcahn School of Medicine at Mount Sinai
Robert RitchEinhorn Clinical Research Center, New York Eye and Ear Infirmary of Mount Sinai
Tin AungSingapore Eye Research Institute
Tin AungDuke-NUS Medical School
Tin AungYong Loo Lin School of Medicine, National University of Singapore
Chiea Chuen KhorGenome Institute of Singapore
Chiea Chuen KhorSingapore Eye Research Institute
Chiea Chuen KhorDuke-NUS Medical School
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