Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3
Open Access
- 11 August 2010
- journal article
- research article
- Published by Springer Science and Business Media LLC in European Journal of Human Genetics
- Vol. 19 (1), 115-117
- https://doi.org/10.1038/ejhg.2010.132
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
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