A Novel Whole Exon Deletion in WWOX Gene Causes Early Epilepsy, Intellectual Disability and Optic Atrophy

The WWOX Gene Modulates High-Density Lipoprotein and Lipid Metabolism

(2014) I. Iatan et al.   Circulation-Cardiovascular Genetics

Common Chromosomal Fragile Site Gene WWOX in Metabolic Disorders and Tumors

(2014) Juan Li et al.   International Journal of Biological Sciences

The supposed tumor suppressor gene WWOX is mutated in an early lethal microcephaly syndrome with epilepsy, growth retardation and retinal degeneration

(2014) Ghada Abdel-Salam et al.   Orphanet Journal of Rare Diseases

A progeroid syndrome with neonatal presentation and long survival maps to 19p13.3p13.2

(2013) Nadia Akawi et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation

(2013) Martial Mallaret et al.   BRAIN

LINS, a modulator of the WNT signaling pathway, is involved in human cognition

(2013) Nadia A Akawi et al.   Orphanet Journal of Rare Diseases

Mutations in DDHD2, Encoding an Intracellular Phospholipase A1, Cause a Recessive Form of Complex Hereditary Spastic Paraplegia

(2012) Janneke H.M. Schuurs-Hoeijmakers et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Delineation of the Clinical, Molecular and Cellular Aspects of NovelJAM3Mutations Underlying the Autosomal Recessive Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Congenital Cataracts

(2012) Nadia A. Akawi et al.   HUMAN MUTATION

A multi-exon deletion within WWOX is associated with a 46,XY disorder of sex development

(2011) Stefan White et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

A copy number variation morbidity map of developmental delay

(2011) Gregory M Cooper et al.   NATURE GENETICS

Mutations of a country: a mutation review of single gene disorders in the United Arab Emirates (UAE)

(2010) Lihadh Al-Gazali et al.   HUMAN MUTATION