Published in
Wiley Open Access, Molecular Genetics and Genomic Medicine, 10(8), 2020
DOI: 10.1002/mgg3.1405
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Transcriptome sequencing identifies a noncoding, deep intronic variant in CLCN7 causing autosomal recessive osteopetrosis
Journal article published in 2020 by
Odelia Chorin,
Naomi Yachelevich,
Khaled Mohamed,
Ilana Moscatelli,
John Pappas,
Kim Henriksen,
Gilad D. Evrony 
This paper is made freely available by the publisher.
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