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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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Foilsithe in:BMC Med Genet
Main Authors: Beke, Artur, Piko, Henriett, Haltrich, Iren, Karcagi, Veronika, Rigo, Janos, Molnar, Maria Judit, Fekete, György
Formáid: Artigo
Teanga:Inglês
Foilsithe: BioMed Central 2018
Ábhair:
Rochtain Ar Líne: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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