Transcriptome sequencing identifies a noncoding, deep intronic variant in CLCN7 causing autosomal recessive osteopetrosis

Abstract Background Over half of children with rare genetic diseases remain undiagnosed despite maximal clinical evaluation and DNA‐based genetic testing. As part of an Undiagnosed Diseases Program applying transcriptome (RNA) sequencing to identify the causes of these unsolved cases, we studied a c...

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Bibliografische gegevens

Hoofdauteurs:	Odelia Chorin, Naomi Yachelevich, Khaled Mohamed, Ilana Moscatelli, John Pappas, Kim Henriksen, Gilad D. Evrony
Formaat:	Artigo
Taal:	Inglês
Gepubliceerd in:	Wiley 2020-10-01
Reeks:	Molecular Genetics & Genomic Medicine
Onderwerpen:	CLCN7 osteopetrosis RNA‐sequencing transcriptomics undiagnosed diseases
Online toegang:	https://doi.org/10.1002/mgg3.1405
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