Ovarian Failure Related to Eukaryotic Initiation Factor 2B Mutations-Reference-Cited by-同舟云学术

Ovarian Failure Related to Eukaryotic Initiation Factor 2B Mutations

Published:2003-06 Issue:6 Volume:72 Page:1544-1550
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Fogli Anne,Rodriguez Diana,Eymard-Pierre Eléonore,Bouhour Françoise,Labauge Pierre,Meaney Brandon F.,Zeesman Susan,Kaneski Christine R.,Schiffmann Raphael,Boespflug-Tanguy Odile

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference28 articles.

1. Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure;Attomäki;Cell,1995

2. Defects in regulation of apoptosis in caspase-2–deficient mice;Bergeron;Genes Dev,1998

3. “vanishing white matter” and ovarian dysgenesis in an infant with cerebro-oculo-facio-skeletal phenotype;Boltshauser;Neuropediatrics,2002

4. Myelinopathia centralis diffusa (VWM disease): evidence of apoptotic oligodendrocyte degeneration in early lesion development;Brück;Ann Neurol,2001

5. Genes and premature ovarian failure;Christin-Maitre;Mol Cell Endocrinol,1998

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