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Title:

Whole genome and exome sequencing identify NDUFV2 mutations as a new cause of progressive cavitating leukoencephalopathy

Document type:
Zeitschriftenaufsatz
Author(s):
Liu, Zhimei; Zhang, Li; Ren, Changhong; Xu, Manting; Li, Shufang; Ban, Rui; Wu, Ye; Chen, Ling; Sun, Suzhen; Elstner, Matthias; Shimura, Masaru; Ogawa-Tominaga, Minako; Murayama, Kei; Shi, Tieliu; Prokisch, Holger; Fang, Fang
Journal title:
Journal of Medical Genetics
Year:
2021
Journal volume:
59
Journal issue:
4
Pages contribution:
351-357
Fulltext / DOI:
doi:10.1136/jmedgenet-2020-107383
Publisher:
BMJ
E-ISSN:
0022-2593; 1468-6244
Date of publication:
02.04.2021
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