Xeroderma pigmentosum group G with severe neurological involvement and features of Cockayne syndrome in infancy.

Zafeiriou, D I

Xeroderma pigmentosum group G with severe neurological involvement and features of Cockayne syndrome in infancy. [electronic resource] - Pediatric research Mar 2001 - 407-12 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

0031-3998

10.1203/00006450-200103000-00016 doi


Alleles
Cockayne Syndrome--genetics
DNA-Binding Proteins--genetics
Endonucleases
Female
Humans
Infant
Mutation
Nuclear Proteins
Transcription Factors
Xeroderma Pigmentosum--genetics