JOURNAL PROFILE
Publications (5)
New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian families
Journal: Neurogenetics
Publication date: 2004
Journal: Neurogenetics
Publication Year: 2004
A new locus (SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum
Journal: Neurogenetics
Publication date: 2010
Journal: Neurogenetics
Publication Year: 2010
A new locus (SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum.
Journal: Neurogenetics
Publication date: 2011
Journal: Neurogenetics
Publication Year: 2011
New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian families.
Journal: Neurogenetics
Publication date: 2004
Journal: Neurogenetics
Publication Year: 2004
Investigating the gut microbiome in schizophrenia cases versus controls: South Africa's version.
Journal: Neurogenetics
Publication date: 2025
Journal: Neurogenetics
Publication Year: 2025