Epilepsy with auditory features: A heterogeneous clinico-molecular disease.
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Enhanced copy number variants detection from whole-exome sequencing data using EXCAVATOR2Spotlight on the June 2015 issueIdentification of DEP domain-containing proteins by a machine learning method and experimental analysis of their expression in human HCC tissues.DEPDC5 mutations in familial and sporadic focal epilepsy.GATOR1 complex: the common genetic actor in focal epilepsies.The role of genetic testing in epilepsy diagnosis and management.Intragenic CNTNAP2 Deletions: A Bridge Too Far?
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Q31120762-E9E81036-166A-4C45-85F0-7BE7C0835621Q36766102-FAD9F0C1-0572-4269-87AB-DF955CCE94ACQ37522321-BFA11282-56EF-4E4D-B17E-2A1384FFB8BBQ38760382-9ABC996E-FA54-4D43-8EE7-6EF2D809FA28Q38840542-B8109EA9-A63A-4B2F-B45C-8C7B80315B2CQ39332606-F49B8B5A-C1DD-4F42-9923-E33EC3EDFD99Q39355257-DDFA22F0-653C-4A5C-AFA3-2553E3B16A42
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Epilepsy with auditory features: A heterogeneous clinico-molecular disease.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Epilepsy with auditory features: A heterogeneous clinico-molecular disease.
@ast
Epilepsy with auditory features: A heterogeneous clinico-molecular disease.
@en
type
label
Epilepsy with auditory features: A heterogeneous clinico-molecular disease.
@ast
Epilepsy with auditory features: A heterogeneous clinico-molecular disease.
@en
prefLabel
Epilepsy with auditory features: A heterogeneous clinico-molecular disease.
@ast
Epilepsy with auditory features: A heterogeneous clinico-molecular disease.
@en
P2093
P2860
P50
P1433
P1476
Epilepsy with auditory features: A heterogeneous clinico-molecular disease
@en
P2093
Chiara Leta
Francesca Bisulli
Giovanni Boero
Giuseppe d'Orsi
Ingrid Scheffer
Laura Licchetta
Marco Seri
Paolo Tinuper
Sara Baldassari
Tommaso Pippucci
P2860
P356
10.1212/NXG.0000000000000005
P577
2015-05-14T00:00:00Z