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Amentia, Familial Cerebellar Diplegia, and Retinitis Pigmentosa.
Proc R Soc Med. 1937 May;30(7):849-50. doi: 10.1177/003591573703000705.
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Familial nephropathy associatdd with retinitis pigmentosa, cerebellar ataxia and skeletal abnormalities.
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[Iridocyclitis in a patient with Behçet's disease and a familial form of retinitis pigmentosa].
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[Familial sector-shaped retinitis pigmentosa].
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[Familial pigmentary retinitis associated with neural amyotrophy].
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引用本文的文献
1
The Genetic Basis of the Hereditary Ataxias.
J R Coll Physicians Lond. 1969 Oct;4(1):88-92.
2
HEREDITARY CEREBELLAR ATAXIA, MENTAL DEFICIENCY, PYRAMIDAL INVOLVEMENT AND MACULAR PIGMENTATION. A BRIEF REVIEW WITH REPORT OF TWO CASES.
Indian J Pediatr. 1964 Dec;31:355-8. doi: 10.1007/BF02762219.
3
Familial cerebro-macular degeneration and ataxia.
J Neurol Neurosurg Psychiatry. 1962 Feb;25(1):63-8. doi: 10.1136/jnnp.25.1.63.
4
A syndrome of severe mental retardation, spasticity, and tapetoretinal degeneration linked to chromosome 15q24.
Am J Hum Genet. 1998 May;62(5):1070-6. doi: 10.1086/301821.
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