Identification of an 85-kb Heterozygous 4p Microdeletion With Full Genome Analysis in Autosomal Dominant Charcot-Marie-Tooth Disease-Reference-Cited by-同舟云学术

Identification of an 85-kb Heterozygous 4p Microdeletion With Full Genome Analysis in Autosomal Dominant Charcot-Marie-Tooth Disease

Published:2023-08 Issue:4 Volume:9 Page:
ISSN:2376-7839
Container-title:Neurology Genetics
language:en
Short-container-title:Neurol Genet

Author:

Hsueh Hsueh Wen¹,Kao Hsiao-Jung¹,Chao Chi-Chao¹,Hsueh Sung-Ju¹,Huang Yu-Ning¹,Lin Wan-Jia¹,Su Jen-Ping¹,Shy Horng-Tzer¹,Yeh Ti-Yen¹,Lin Cheng-Chen¹,Kwok Pui-Yan¹,Lee Ni-Chung¹,Hsieh Sung-Tsang¹^ORCID

Affiliation:

1. From the Department of Neurology (H.W.H., C.-C.C., Y.-N.H., S.-T.H.), Department of Anatomy and Cell Biology (H.W.H., H.-T.S., T.-Y.Y., C.-C.L., S.-T.H.), National Taiwan University College of Medicine; Institute of Biomedical Sciences (H.-J.K., W.-J.L., J.-P.S., P.-Y.K.), Academia Sinica, Taipei; Department of Neurology (S.-J.H.), National Taiwan University Hospital Yunlin Branch; Institute for Human Genetics (P.-Y.K.), Cardiovascular Research Institute, and Department of Dermatology, University of...

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics (clinical),Neurology (clinical)

Link

https://www.neurology.org/doi/pdfdirect/10.1212/NXG.0000000000200078

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