New variants, challenges and pitfalls in DMD genotyping: implications in diagnosis, prognosis and therapy-Reference-Cited by-同舟云学术

New variants, challenges and pitfalls in DMD genotyping: implications in diagnosis, prognosis and therapy

Published:2014-07-10 Issue:8 Volume:59 Page:454-464
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Santos Rosário,Gonçalves Ana,Oliveira Jorge,Vieira Emília,Vieira José Pedro,Evangelista Teresinha,Moreno Teresa,Santos Manuela,Fineza Isabel,Bronze-da-Rocha Elsa

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/jhg201454.pdf

Reference39 articles.

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4. Cotton, S., Voudouris, N. J. & Greenwood, K. M. Intelligence and Duchenne muscular dystrophy: full-scale, verbal, and performance intelligence quotients. Dev. Med. Child. Neurol. 43, 497–501 (2001).

5. Koenig, M., Hoffman, E. P., Bertelson, C. J., Monaco, A. P., Feener, C. & Kunkel, L. M. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. Cell 50, 509–517 (1987).

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