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Duplicate report crossing over in Norrie disease family

✍ Scribed by Ngo, Julielani ;Spence, M. Anne ;Cortessis, Victoria ;Bateman, J. Bronwyn ;Sparkes, Robert S.

Book ID
101445026
Publisher
John Wiley and Sons
Year
1989
Tongue
English
Weight
47 KB
Volume
33
Category
Article
ISSN
0148-7299

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πŸ“œ SIMILAR VOLUMES

NDP gene mutations in 14 French families
NDP gene mutations in 14 French families with Norrie disease
✍ Ghislaine Royer; Sylvain Hanein; ValΓ©rie Raclin; Nadine Gigarel; Jean-Michel Roz πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 29 KB

Norrie disease is a rare X-inked recessive condition characterized by congenital blindness and occasionally deafness and mental retardation in males. This disease has been ascribed to mutations in the NDP gene on chromosome Xp11.1. Previous investigations of the NDP gene have identified largely sixt