Epilepsy in Mowat-Wilson syndrome: Delineation of the electroclinical phenotype-Reference-Cited by-同舟云学术

Epilepsy in Mowat-Wilson syndrome: Delineation of the electroclinical phenotype

Published:2013-01-15 Issue:2 Volume:161 Page:273-284
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Cordelli Duccio Maria,Garavelli Livia,Savasta Salvatore,Guerra Azzurra,Pellicciari Alessandro,Giordano Lucio,Bonetti Silvia,Cecconi Ilaria,Wischmeijer Anita,Seri Marco,Rosato Simonetta,Gelmini Chiara,Della Giustina Elvio,Ferrari Anna Rita,Zanotta Nicoletta,Epifanio Roberta,Grioni Daniele,Malbora Baris,Mammi Isabella,Mari Francesca,Buoni Sabrina,Mostardini Rosa,Grosso Salvatore,Pantaleoni Chiara,Doz Morena,Poch-Olivé Maria Luisa,Rivieri Francesca,Sorge Giovanni,Simonte Graziella,Licata Francesca,Tarani Luigi,Terazzi Emanuela,Mazzanti Laura,Cerruti Mainardi Paola,Boni Antonella,Faravelli Francesca,Grasso Marina,Bianchi Paolo,Zollino Marcella,Franzoni Emilio

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.35717/fullpdf

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4. Spectrum of epilepsy and electroencephalogram patterns in Wolf-Hirschhorn syndrome: Experience with 87 patients;Battaglia;Dev Med Child Neurol,2009

5. Loss-of-function mutations in SIP1 Smad interacting protein 1 results in a syndromic Hirschsprung disease;Cacheux;Hum Mol Genet,2001

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