19960070

Source:http://linkedlifedata.com/resource/pubmed/id/19960070

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015576, umls-concept:C0017337, umls-concept:C0019904, umls-concept:C0026882, umls-concept:C0035334, umls-concept:C0240620, umls-concept:C0425375, umls-concept:C0441748, umls-concept:C2355587
pubmed:dateCreated	2009-12-4
pubmed:abstractText	To identify the gene mutations responsible for autosomal recessive retinitis pigmentosa (arRP) in Pakistani families.
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/19960070-11891118, http://linkedlifedata.com/resource/pubmed/commentcorrection/19960070-12015282, http://linkedlifedata.com/resource/pubmed/commentcorrection/19960070-12876833, http://linkedlifedata.com/resource/pubmed/commentcorrection/19960070-1303237, http://linkedlifedata.com/resource/pubmed/commentcorrection/19960070-15327956, http://linkedlifedata.com/resource/pubmed/commentcorrection/19960070-15347576, http://linkedlifedata.com/resource/pubmed/commentcorrection/19960070-15726226, http://linkedlifedata.com/resource/pubmed/commentcorrection/19960070-15767903, http://linkedlifedata.com/resource/pubmed/commentcorrection/19960070-16737970, http://linkedlifedata.com/resource/pubmed/commentcorrection/19960070-17289671, http://linkedlifedata.com/resource/pubmed/commentcorrection/19960070-17715341, http://linkedlifedata.com/resource/pubmed/commentcorrection/19960070-17943122, http://linkedlifedata.com/resource/pubmed/commentcorrection/19960070-1862076, http://linkedlifedata.com/resource/pubmed/commentcorrection/19960070-6702974, http://linkedlifedata.com/resource/pubmed/commentcorrection/19960070-7093178, http://linkedlifedata.com/resource/pubmed/commentcorrection/19960070-7887430, http://linkedlifedata.com/resource/pubmed/commentcorrection/19960070-7987385, http://linkedlifedata.com/resource/pubmed/commentcorrection/19960070-8236849, http://linkedlifedata.com/resource/pubmed/commentcorrection/19960070-8473105, http://linkedlifedata.com/resource/pubmed/commentcorrection/19960070-8885257, http://linkedlifedata.com/resource/pubmed/commentcorrection/19960070-9475085, http://linkedlifedata.com/resource/pubmed/commentcorrection/19960070-9540407
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9605351
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Rhodopsin
pubmed:status	MEDLINE
pubmed:issn	1090-0535
pubmed:author	pubmed-author:AzamMaleehaM, pubmed-author:BokhariHabibH, pubmed-author:CollinRob W JRW, pubmed-author:CremersFrans P MFP, pubmed-author:GalAndreasA, pubmed-author:HussainAlamdarA, pubmed-author:KhanMuhammad ImranMI, pubmed-author:KhanMuhammad ShakilMS, pubmed-author:OrthUlrikeU, pubmed-author:QamarRaheelR, pubmed-author:SadequeAhmedA, pubmed-author:ShahSyed Tahir AbbasST, pubmed-author:den HollanderA IAI, pubmed-author:van GenderenMaria MMM
pubmed:issnType	Electronic
pubmed:volume	15
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	2526-34
pubmed:dateRevised	2010-9-27
pubmed:meshHeading	pubmed-meshheading:19960070-Alleles, pubmed-meshheading:19960070-Amino Acid Sequence, pubmed-meshheading:19960070-Amino Acid Substitution, pubmed-meshheading:19960070-Asian Continental Ancestry Group, pubmed-meshheading:19960070-Base Sequence, pubmed-meshheading:19960070-Chi-Square Distribution, pubmed-meshheading:19960070-Family, pubmed-meshheading:19960070-Female, pubmed-meshheading:19960070-Fundus Oculi, pubmed-meshheading:19960070-Genes, Recessive, pubmed-meshheading:19960070-Haplotypes, pubmed-meshheading:19960070-Homozygote, pubmed-meshheading:19960070-Humans, pubmed-meshheading:19960070-Male, pubmed-meshheading:19960070-Microsatellite Repeats, pubmed-meshheading:19960070-Molecular Sequence Data, pubmed-meshheading:19960070-Mutation, pubmed-meshheading:19960070-Pakistan, pubmed-meshheading:19960070-Pedigree, pubmed-meshheading:19960070-Polymorphism, Single Nucleotide, pubmed-meshheading:19960070-Retinitis Pigmentosa, pubmed-meshheading:19960070-Rhodopsin, pubmed-meshheading:19960070-Sequence Analysis
pubmed:year	2009
pubmed:articleTitle	A homozygous p.Glu150Lys mutation in the opsin gene of two Pakistani families with autosomal recessive retinitis pigmentosa.
pubmed:affiliation	Department of Biosciences, COMSATS Institute of Information Technology, Islamabad, Pakistan.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't