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Study of patterns of inheritance of premature ovarian failure syndrome carrying maternal and paternal premutations
BACKGROUND: Premature ovarian failure / primary ovarian insufficiency (POF/POI) associated with the mutations of the FMR1 (Fragile-X Mental Retardation 1) gene belongs to the group of the so-called trinucleotide expansion diseases. Our aim was to analyse the relationship between the paternally inher...
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| Pubblicato in: | BMC Med Genet |
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| Autori principali: | , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6038184/ https://ncbi.nlm.nih.gov/pubmed/29986653 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-018-0634-5 |
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