Associated Papers
WWOX Loss of Function in Neurodevelopmental and Neurodegenerative Disorders.
Aldaz CM et al.
International Journal of Molecular Sciences, 2020
Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease.
Jolly A et al.
The Journal of Clinical Endocrinology and Metabolism, 2019
WWOX somatic ablation in skeletal muscles alters glucose metabolism.
Abu-Remaileh M et al.
Molecular Metabolism, 2019
30755385 (PubMed )
Supplement: mmc1.pdf
C6orf10 Low-Frequency and Rare Variants in Italian Multiple Sclerosis Patients.
Ziliotto N et al.
Frontiers in Genetics, 2019
Epigenetic and genetic alterations affect the WWOX gene in head and neck squamous cell carcinoma.
Ekizoglu S et al.
Plos One, 2015
Identification of homozygous deletions at chromosome 16q23 in aflatoxin B1 exposed hepatocellular carcinoma.
Yakicier MC et al.
Oncogene, 2001
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