Sequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotype

Earlier reports demonstrated a key role of Cdkn1b during mouse ovarian development. In this study, the sequencing analysis of the complete coding region of this gene in a panel of premature ovarian failure patients and control subjects reveals a novel mutation potentially related to the phenotype. ©...

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Autores:

Tipo de recurso:

Fecha de publicación:

2011

Institución:

Universidad del Rosario

Repositorio:

Repositorio EdocUR - U. Rosario

Idioma:

eng

OAI Identifier:

oai:repository.urosario.edu.co:10336/24059

Acceso en línea:

https://doi.org/10.1016/j.fertnstert.2011.04.045
https://repository.urosario.edu.co/handle/10336/24059

Palabra clave:

Cyclin dependent kinase inhibitor 1B
Follitropin
Adult
Article
Autoimmune disease
Controlled study
Female
Female infertility
Follitropin blood level
Gene mutation
Genetic analysis
Genetic code
Human
Informed consent
Karyotype
Major clinical study
Ovary development
Ovary insufficiency
Pelvis surgery
Phenotype
Premature ovarian failure
Priority journal
Sequence analysis
Single nucleotide polymorphism
CDKN1B
Mutations
Premature ovarian failure (POF)
Sequencing

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