Genetic analysis of adult leukoencephalopathy patients using a custom‐designed gene panel-Reference-Cited by-同舟云学术

Genetic analysis of adult leukoencephalopathy patients using a custom‐designed gene panel

Published:2018-06-08 Issue:2 Volume:94 Page:232-238
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Kunii M.¹^ORCID,Doi H.¹,Ishii Y.¹,Ohba C.¹,Tanaka K.¹,Tada M.¹,Fukai R.¹,Hashiguchi S.¹,Kishida H.²,Ueda N.²,Kudo Y.³,Kugimoto C.³,Nakano T.⁴,Udaka N.⁵,Miyatake S.⁶,Miyake N.⁶^ORCID,Saitsu H.⁶,Ito Y.⁷,Takahashi K.¹,Nakamura H.¹,Tomita‐Katsumoto A.¹,Takeuchi H.¹,Koyano S.¹,Matsumoto N.⁶,Tanaka F.¹

Affiliation:

1. Department of Neurology and Stroke Medicine Yokohama City University Yokohama Japan

2. Department of Neurology Yokohama City University Medical Center Yokohama Japan

3. Department of Neurology Yokohama City Stroke, Nerve Backbone Center Yokohama Japan

4. Department of Neurology and Stroke Medicine Yokohama Sakae Kyosai Hospital Yokohama Japan

5. Department of Pathology Yokohama City University Yokohama Japan

6. Department of Human Genetics Yokohama City University Yokohama Japan

7. Department of Neurology Toyota Memorial Hospital Toyota Japan

Funder

Japan Science and Technology Agency

Yokohama Foundation for Advanced Medical Science

Ichiro Kanehara Foundation for the Promotion of Medical Sciences and Medical Care

Takeda Science Foundation

Ministry of Health, Labour and Welfare

Japan Agency for Medical Research and Development

Japan Society for the Promotion of Science

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.13371

Reference28 articles.

1. Targeted capture and sequencing for detection of mutations causing early onset epileptic encephalopathy

2. Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment.

3. Invited Article: An MRI-based approach to the diagnosis of white matter disorders

4. MR signal abnormalities at 1.5 T in Alzheimer's dementia and normal aging

5. ANKRD11 variants cause variable clinical features associated with KBG syndrome and Coffin–Siris-like syndrome

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