19564592

Source:http://linkedlifedata.com/resource/pubmed/id/19564592

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0085584, umls-concept:C0205082, umls-concept:C1096063, umls-concept:C1420484, umls-concept:C1833334
pubmed:issue	1
pubmed:dateCreated	2009-6-30
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/19564592-18809835
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0401060
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/CDKL5 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Genetic Markers, http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	1526-632X
pubmed:author	pubmed-author:Bahi-BuissonNN, pubmed-author:BienvenuTT, pubmed-author:BiethEE, pubmed-author:ChaixYY, pubmed-author:ChellyJJ, pubmed-author:FichouYY, pubmed-author:GirardBB, pubmed-author:NectouxJJ
pubmed:issnType	Electronic
pubmed:day	7
pubmed:volume	73
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	77-8; author reply 78
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:19564592-Age of Onset, pubmed-meshheading:19564592-Amino Acid Substitution, pubmed-meshheading:19564592-Brain Diseases, Metabolic, pubmed-meshheading:19564592-Cerebral Cortex, pubmed-meshheading:19564592-Child, Preschool, pubmed-meshheading:19564592-Cohort Studies, pubmed-meshheading:19564592-DNA Mutational Analysis, pubmed-meshheading:19564592-Developmental Disabilities, pubmed-meshheading:19564592-Disease Progression, pubmed-meshheading:19564592-Epilepsy, pubmed-meshheading:19564592-Female, pubmed-meshheading:19564592-Genetic Markers, pubmed-meshheading:19564592-Genetic Predisposition to Disease, pubmed-meshheading:19564592-Genetic Testing, pubmed-meshheading:19564592-Genotype, pubmed-meshheading:19564592-Humans, pubmed-meshheading:19564592-Male, pubmed-meshheading:19564592-Movement Disorders, pubmed-meshheading:19564592-Muscle Hypotonia, pubmed-meshheading:19564592-Mutation, pubmed-meshheading:19564592-Polymorphism, Single Nucleotide, pubmed-meshheading:19564592-Protein-Serine-Threonine Kinases
pubmed:year	2009
pubmed:articleTitle	Re: CDKL5 mutations in boys with severe encephalopathy and early-onset intractable epilepsy.
pubmed:publicationType	Letter, Comment, Case Reports, Research Support, Non-U.S. Gov't