Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa-Reference-Cited by-同舟云学术

Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa

Published:2018-04 Issue:4 Volume:102 Page:713
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Angius Andrea,Uva Paolo,Buers Insa,Oppo Manuela,Puddu Alessandro,Onano Stefano,Persico Ivana,Loi Angela,Marcia Loredana,Höhne Wolfgang,Cuccuru Gianmauro,Fotia Giorgio,Deiana Manila,Marongiu Mara,Atalay Hatice Tuba,Inan Sibel,El Assy Osama,Smit Leo M.E.,Okur Ilyas,Boduroglu Koray,Utine Gülen Eda,Kılıç Esra,Zampino Giuseppe,Crisponi Giangiorgio,Crisponi Laura,Rutsch Frank

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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