Hunter and fragile-X syndromes in a family with Xq27.3-q28 deletion that involves FMR1 and IDS genes

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Bibliographic Details
Published in:European journal of paediatric neurology 2017-06, Vol.21, p.e139-e139
Main Authors: Aguilera-Albesa, S, Mosquera-Gorostidi, A, Naberan-Mardaras, I, Gorria-Redondo, N, Urriza-Ripa, I, Yoldi-Petri, M.E, Ramos-Arroyo, M.A, Coll, M.J, Aznal, E, Sanchez-Valverde, F
Format: Article
Language:English
Subjects:
Neurology
Pediatrics
Online Access:Get full text
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ISSN:1090-3798
1532-2130
DOI:10.1016/j.ejpn.2017.04.1049