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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Detalles Bibliográficos
Autores principales: Beke, Artur, Piko, Henriett, Haltrich, Iren, Karcagi, Veronika, Rigo, Janos, Molnar, Maria Judit, Fekete, György
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6038184/
https://www.ncbi.nlm.nih.gov/pubmed/29986653
http://dx.doi.org/10.1186/s12881-018-0634-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6038184/
https://www.ncbi.nlm.nih.gov/pubmed/29986653
http://dx.doi.org/10.1186/s12881-018-0634-5

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