Published in
Wiley, Human Mutation: Variation, Informatics and Disease, 8(42), p. 969-977, 2021
DOI: 10.1002/humu.24220
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Genetic pleiotropy of ERCC6 loss‐of‐function and deleterious missense variants links retinal dystrophy, arrhythmia, and immunodeficiency in diverse ancestries
Journal article published in 2021 by
Iain S. Forrest 
,
Kumardeep Chaudhary ,
Ha My T. Vy,
Shantanu Bafna,
Soyeon Kim,
Hong‐Hee Won,
Ruth J. F. Loos,
Judy Cho,
Louis R. Pasquale,
Girish N. Nadkarni,
Ghislain Rocheleau,
Ron Do
,
Kumardeep Chaudhary ,
Ha My T. Vy,
Shantanu Bafna,
Soyeon Kim,
Hong‐Hee Won,
Ruth J. F. Loos,
Judy Cho,
Louis R. Pasquale,
Girish N. Nadkarni,
Ghislain Rocheleau,
Ron Do
This paper was not found in any repository, but could be made available legally by the author.
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