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          Institute: MPI für molekulare Genetik     Collection: Department of Human Molecular Genetics     Display Documents



  history
ID: 469307.0, MPI für molekulare Genetik / Department of Human Molecular Genetics
CDKL5 truncation due to a t(X;2)(p22.1;p25.3) in a girl with X-linked infantile spasm syndrome
Authors:Córdova-Fletes, C.; Rademacher, N.; Müller, I.; Mundo-Ayala, J. N.; Morales-Jeanhs, E. A.; García-Ortiz, J. E.; León-Gil, A.; Rivera, H.; Domínguez, M. G.; Kalscheuer, V. M.
Language:English
Date of Publication (YYYY-MM-DD):2010-01-01
Title of Journal:Clinical Genetics
Journal Abbrev.:Clin Genet
Volume:77
Issue / Number:1
Start Page:92
End Page:96
Copyright:© 2010 John Wiley & Sons A/S
Review Status:not specified
Audience:Experts Only
Comment of the Author/Creator:email: kalscheu@molgen.mpg.de
External Publication Status:published
Document Type:Article
Communicated by:Hans-Hilger Ropers
Affiliations:MPI für molekulare Genetik
External Affiliations:División de Genética, Centro de Investigación Biomédica de Occidente, CMNO-IMSS, 44340 Guadalajara, México
Doctorado en Genética Humana, Universidad de Guadalajara, 44340 Guadalajara, México
Departamento de Neurología y Neurocirugía Pediátrica, UMAE Hospital de Pediatría, CMNO-IMSS, 44340 Guadalajara, México
Identifiers:DOI:10.1111/j.1399-0004.2009.01286.x
ISSN:0009-9163
URL:http://www3.interscience.wiley.com/cgi-bin/fulltex...
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