Diagnosis of becker muscular dystrophy: Results of Re-analysis of DNA samples

Autor: Straathof, C.S., Heusden, D. Van, Ippel, P.F., Post, J.G., Voermans, N.C., Visser, M. de, Brusse, E., Bergen, J.C. van den, Kooi, A.J. van der, Verschuuren, J.J., Ginjaar, H.B.

Publikováno v: Muscle & nerve, 53(1), 44-48. John Wiley and Sons Inc.
Muscle & Nerve, 53(1), 44. John Wiley and Sons Inc.
Muscle and Nerve, 53, 44-8
Muscle & Nerve, 53(1), 44-48. John Wiley & Sons Inc.
Muscle and Nerve, 53, 1, pp. 44-8

Item does not contain fulltext INTRODUCTION: The phenotype of Becker muscular dystrophy (BMD) is highly variable, and the disease may be underdiagnosed. We searched for new mutations in the DMD gene in a cohort of previously undiagnosed patients who

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::7f952fb48b193831d1e74b03f44eb03b
https://hdl.handle.net/2066/167723