Next Generation Mendelian Genetics: Kabuki Syndrome

Study ID Alternative Stable ID Type
phs000295 Exome Sequencing

Study Description

The ultimate purpose of this research is to identify genes causing hereditary disorders. We are scaling a new approach to identify the candidate genes and gene mutations that underlie rare human Mendelian (a set of primary tenets relating to the transmission of hereditary characteristics from parent to child) diseases by using exome (protein coding segments of DNA) resequencing.

The exome sequences of ten unrelated individuals with a diagnosis of Kabuki Syndrome (OMIM: 147920) were obtained by massively parallel DNA sequencing.

Archive Link Archive Accession
dbGaP phs000295

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