Null and missense mutations of ERI1 cause a recessive phenotypic dichotomy in humans-Reference-Cited by-同舟云学术

Null and missense mutations of ERI1 cause a recessive phenotypic dichotomy in humans

Published:2023-07 Issue:7 Volume:110 Page:1068-1085
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Guo Long^ORCID,Salian Smrithi,Xue Jing-yi,Rath Nicola,Rousseau Justine,Kim Hyunyun,Ehresmann Sophie,Moosa Shahida,Nakagawa Norio,Kuroda Hiroshi,Clayton-Smith Jill,Wang Juan,Wang Zheng,Banka Siddharth,Jackson Adam,Zhang Yan-min,Wei Zhen-jie,Hüning Irina,Brunet Theresa,Ohashi Hirofumi,Thomas Molly F.,Bupp Caleb,Miyake Noriko,Matsumoto Naomichi,Mendoza-Londono Roberto,Costain Gregory,Hahn Gabriele,Di Donato Nataliya,Yigit Gökhan,Yamada Takahiro,Nishimura Gen,Ansel K Mark,Wollnik Bernd,Hrabě de Angelis Martin,Mégarbané André,Rosenfeld Jill A.,Heissmeyer Vigo,Ikegawa Shiro,Campeau Philippe M.^ORCID

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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