Human Genome Epidemiology Literature Finder
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Query Trace: Gonadal Dysgenesis and CLPP[original query] |
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A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family. Journal of clinical research in pediatric endocrinology 2016 Apr . Dursun Fatma, Mohamoud Hussein Sheikh Ali, Karim Noreen, Naeem Muhammad, Jelani Musharraf, K?rm?z?bekmez Hev |
- Page last reviewed:Feb 1, 2024
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