Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts, unlinked to the LAMA2, FCMD, MEB and CMD1B loci, in three Tunisian patients. [electronic resource]
Producer: 20030312Description: 4-12 p. digitalISSN:- 0960-8966
- Brain -- pathology
- Central Nervous System Cysts -- etiology
- Child
- Child, Preschool
- Chromosome Mapping
- Female
- Fluorescent Antibody Technique
- Genetic Linkage -- genetics
- Genetic Markers
- Humans
- Intellectual Disability -- etiology
- Laminin -- deficiency
- Lod Score
- Magnetic Resonance Imaging
- Male
- Membrane Proteins
- Muscle, Skeletal -- metabolism
- Muscular Dystrophies -- complications
- Pedigree
- Proteins -- genetics
- Tunisia
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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