Schizophrenia and mental retardation associated in a pedigree with retinitis pigmentosa and sensorineural deafness
β Scribed by Sharp, C. W. ;Muir, W. J. ;Blackwood, D. H. R. ;Walker, M. ;Gosden, C. ;St. Clair, D. M.
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 696 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0148-7299
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π SIMILAR VOLUMES
We have detected a novel mitochondrial mutation in a maternal pedigree, at least 13 of whose members have sensorineural hearing loss of varying severity, but who exhibit no other pathological features. The mutation, at np 7445, converts the 3' terminal T residue of tRNA-ser(UCN) to a C, and also bri
Weak support for linkage of schizophrenia to proximal Xq has previously been reported. In addition, an increased prevalence of thyroid disorder has been noted in families of individuals with schizophrenia. Recently, a gene mapped to Xq13 termed HOPA has been found to be associated with mental retard