Greater prevalence of PROKR2 mutations in Kallmann syndrome patients from the Maghreb than in European patients. [electronic resource]
Producer: 20131216Description: 805-9 p. digitalISSN:- 1479-683X
- Adult
- Africa, Northern
- Aged
- Arabs -- genetics
- Europe
- Exons
- Extracellular Matrix Proteins -- genetics
- Female
- Fibroblast Growth Factor 8 -- genetics
- Gastrointestinal Hormones -- genetics
- Gene Frequency
- Humans
- Introns
- Kallmann Syndrome -- epidemiology
- Male
- Middle Aged
- Mutation
- Nerve Tissue Proteins -- genetics
- Neuropeptides -- genetics
- Prevalence
- Receptor, Fibroblast Growth Factor, Type 1 -- genetics
- Receptors, G-Protein-Coupled -- genetics
- Receptors, Peptide -- genetics
- Sequence Analysis, DNA
- White People -- genetics
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Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
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