Homozygosity mapping through whole genome analysis identifies a COL18A1 mutation in an Indian family presenting with an autosomal recessive neurological disorder.

Source:http://linkedlifedata.com/resource/pubmed/id/19160445

Am. J. Med. Genet. B Neuropsychiatr. Genet. 2009 Oct 5 150B 7 993-7

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19160445