𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM

✍ Scribed by K.L. Friend; D. Crimmins; T.G. Phan; C.M. Sue; A. Colley; V.S.C. Fung; J.G.L. Morris; G.R. Sutherland; R.I. Richards


Publisher
Springer
Year
1999
Tongue
English
Weight
105 KB
Volume
105
Category
Article
ISSN
0340-6717

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Mutational screening of the RB1 gene in
✍ Velamakanni Saroj Kiran; Chitra Kannabiran; Kalyana Chakravarthi; Geeta K. Vemug πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 37 KB πŸ‘ 1 views

Retinoblastoma is the most common primary intraocular malignancy in children, caused by inactivation of the RB1 gene on chromosome 13. We carried out a mutational screen of the exons and promoter of the RB1 gene in Indian patients with retinoblastoma in order to determine the range of mutations givi