Homozygosity mapping in a family presenting with schizophrenia, epilepsy and hearing impairment

European Journal of Human Genetics

Volumn 16, Issue 6, 2008, Pages 750-758

  Knight, Helen M ^a   Maclean, Alan ^b   Irfan, Muhammad ^c   Naeem, Farooq ^d   Cass, Stephen ^b   Pickard, Benjamin S ^b   Muir, Walter J ^a   Blackwood, Douglas H R ^a   Ayub, Muhammad ^e  

^a UNIVERSITY OF EDINBURGH   (United Kingdom)

^b UNIVERSITY OF EDINBURGH   (United Kingdom)

^c Lahore Institute of Research and Development   (Pakistan)

^d FATIMA JINNAH MEDICAL COLLEGE   (Pakistan)

^e St Lukes Hospital   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVATING TRANSCRIPTION FACTOR 4; CALCIUM CHANNEL L TYPE; GENE PRODUCT; PROTEIN CACNG2; PROTEIN KCNF1; VOLTAGE GATED POTASSIUM CHANNEL;

ARTICLE; CHROMOSOME 22Q; CHROMOSOME 2P; CLINICAL ARTICLE; CONSANGUINEOUS MARRIAGE; EPILEPSY; GENE LOCUS; GENE MAPPING; GENETIC SCREENING; HEARING IMPAIRMENT; HOMOZYGOSITY; HUMAN; MUTATIONAL ANALYSIS; PAKISTAN; PHENOTYPE; PRIORITY JOURNAL; SCHIZOPHRENIA; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 2; CHROMOSOMES, HUMAN, PAIR 22; EPILEPSY; FEMALE; HEARING DISORDERS; HOMOZYGOTE; HUMANS; MALE; MUTATION; PEDIGREE; POLYMORPHISM, SINGLE NUCLEOTIDE; SCHIZOPHRENIA;

EID: 44449116152     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2008.11     Document Type: Article

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