Erratum: XLID-Causing Mutations and Associated Genes Challenged in Light of Data From Large-Scale Human Exome Sequencing(S0002929713002826)(10.1016/j.ajhg.2013.06.013);XLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencing

American Journal of Human Genetics

Volumn 93, Issue 2, 2013, Pages 368-383

  Piton, Amélie ^a,b   Redin, Claire ^a,b   Mandel, Jean Louis ^a,b,c  

^a UNIVERSITÉ DE STRASBOURG   (France)

^b l'alimentation et l'Environnement   (France)

^c UNIVERSITY HOSPITAL OF STRASBOURG   (France)

Author keywords

[No Author keywords available]

Indexed keywords

AMINE OXIDASE (FLAVIN CONTAINING) ISOENZYME A; ANGIOTENSIN RECEPTOR; ANGIOTENSIN RECEPTOR 2; GUANINE NUCLEOTIDE EXCHANGE FACTOR; GUANINE NUCLEOTIDE EXCHANGE FACTOR 6; NUCLEAR FACTOR; NUCLEAR RNA EXPORT FACTOR 5; TRANSCRIPTION FACTOR YY1; UBIQUITIN PROTEIN LIGASE E3; UNCLASSIFIED DRUG; UROKINASE RECEPTOR; ZINC FINGER PROTEIN; ZINC FINGER PROTEIN 41; ZINC FINGER PROTEIN 674;

AGGRESSION; ARTICLE; AUTISM; CENTRONUCLEAR MYOPATHY; CHROMOSOME MUTATION; COGNITIVE DEFECT; COMPARATIVE GENOMIC HYBRIDIZATION; FACIOGENITAL DYSPLASIA; FALSE POSITIVE RESULT; FRAMESHIFT MUTATION; GENE MUTATION; GENETIC ASSOCIATION; HIGH THROUGHPUT SEQUENCING; HUMAN; INTELLECTUAL IMPAIRMENT; LARGE SCALE HUMAN EXOME SEQUENCING; LINKAGE ANALYSIS; MISSENSE MUTATION; NONHUMAN; NONSENSE MUTATION; NORRIE DISEASE; NUCLEOTIDE SEQUENCE; PATHOGENICITY; PERICENTRIC CHROMOSOME INVERSION; PHENOTYPE; POINT MUTATION; PRIORITY JOURNAL; REPLICATION STUDY; RETINITIS PIGMENTOSA; SEX RATIO; SPONTANEOUS MUTATION; X CHROMOSOME; X CHROMOSOME LINKED DISORDER;

EID: 84881618216     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2013.07.019     Document Type: Erratum

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