Congenital X-linked ataxia, progressive myoclonic encephalopathy, macular degeneration and recurrent infections-Reference-Cited by-同舟云学术

Congenital X-linked ataxia, progressive myoclonic encephalopathy, macular degeneration and recurrent infections

Published:1992-04-15 Issue:1-2 Volume:43 Page:443-451
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Bertini Enrico,Cusmai Raffaella,de Saint Basile Genevieve,Le Deist Françoise,Di Capua Matteo,Gaggero Di Roberto,Dionisi-Vici Carlo,Santillo Clemente,Caniglia Maurizio

Publisher

Wiley

Subject

Genetics (clinical)

Reference14 articles.

1. Heterogeneity of X-linked recessive (Spino)cerebellar ataxia with or without spastic diplegia

2. (1977) Agenesis septi pellucidi, cavum septi pellucidi, cavum vergae and cavum veli interposti. In (eds): “Handbook of Neurology (vol. 30): Congenital Malformations of the Brain and Skull, part I.” Amsterdam, The Netherlands: Elsevier/North Holland Biomedical: pp. 299-336.

3. Progressive Myoclonic Encephalopathy in X-Linked Hypogamma-Globulinemia

4. Agenesis of the corpus callosum, combined immunodeficiency, bilateral cataract, and hypopigmentation in two brothers

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