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

Diego Ojeda; Besma Lakhal; Dora Janneth Fonseca; Rim Braham; Hanne Landolsi; Heidi Eliana Mateus; Carlos Martín Restrepo; Hatem Elghezal; Ali Saâd; Paul Laissue

doi:10.1016/j.fertnstert.2011.04.045

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

Diego Ojeda
, Besma Lakhal
, Dora Janneth Fonseca
, Rim Braham
, Hanne Landolsi
, Heidi Eliana Mateus
, Carlos Martín Restrepo
, Hatem Elghezal
, Ali Saâd
, Paul Laissue

Research output: Contribution to Journal › Research Article › peer-review

17 Scopus citations

Abstract

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.

Translated title of the contribution	El análisis de secuencia del gen CDKN1B en pacientes con insuficiencia ovárica prematura revela una nueva mutación potencialmente relacionada con el fenotipo
Original language	English (US)
Article number	e1
Pages (from-to)	2658-2660
Number of pages	4
Journal	Fertility and Sterility
Volume	95
Issue number	8
DOIs	https://doi.org/10.1016/j.fertnstert.2011.04.045
State	Published - Jun 30 2011

All Science Journal Classification (ASJC) codes

Genetics(clinical)

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1016/j.fertnstert.2011.04.045

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Ojeda, D., Lakhal, B., Fonseca, D. J., Braham, R., Landolsi, H., Mateus, H. E., Restrepo, C. M., Elghezal, H., Saâd, A., & Laissue, P. (2011). Sequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotype. Fertility and Sterility, 95(8), 2658-2660. Article e1. https://doi.org/10.1016/j.fertnstert.2011.04.045

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

abstract = "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.",

author = "Diego Ojeda and Besma Lakhal and Fonseca, \{Dora Janneth\} and Rim Braham and Hanne Landolsi and Mateus, \{Heidi Eliana\} and Restrepo, \{Carlos Mart{\'i}n\} and Hatem Elghezal and Ali Sa{\^a}d and Paul Laissue",

note = "{\textcopyright} 2011 by American Society for Reproductive Medicine.",

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doi = "10.1016/j.fertnstert.2011.04.045",

language = "English (US)",

volume = "95",

pages = "2658--2660",

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Ojeda, D, Lakhal, B, Fonseca, DJ, Braham, R, Landolsi, H, Mateus, HE, Restrepo, CM, Elghezal, H, Saâd, A & Laissue, P 2011, 'Sequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotype', Fertility and Sterility, vol. 95, no. 8, e1, pp. 2658-2660. https://doi.org/10.1016/j.fertnstert.2011.04.045

TY - JOUR

T1 - Sequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotype

AU - Ojeda, Diego

AU - Lakhal, Besma

AU - Fonseca, Dora Janneth

AU - Braham, Rim

AU - Landolsi, Hanne

AU - Mateus, Heidi Eliana

AU - Restrepo, Carlos Martín

AU - Elghezal, Hatem

AU - Saâd, Ali

AU - Laissue, Paul

PY - 2011/6/30

Y1 - 2011/6/30

N2 - 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.

AB - 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.

U2 - 10.1016/j.fertnstert.2011.04.045

DO - 10.1016/j.fertnstert.2011.04.045

M3 - Research Article

SN - 0015-0282

VL - 95

SP - 2658

EP - 2660

JO - Fertility and Sterility

JF - Fertility and Sterility

IS - 8

M1 - e1

ER -

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

Abstract

All Science Journal Classification (ASJC) codes

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