Two female patients with Xq27.3q28 deletion and skewed X-inactivation display similar phenotypes as hunter syndrome

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Bibliographic Details
Published in:Journal of the neurological sciences 2017-10, Vol.381, p.194-194
Main Authors: Katoh, K., Aiba, K., Fukushi, D., Suzuki, Y., Yamada, K., Wakamatsu, N.
Format: Article
Language:English
Online Access:Get full text
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ISSN:0022-510X
1878-5883
DOI:10.1016/j.jns.2017.08.554