A case of paternally inherited congenital myotonic dystrophy.

Author:

Nakagawa M,Yamada H,Higuchi I,Kaminishi Y,Miki T,Johnson K,Osame M

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference16 articles.

1. Myotonic dystrophy;Harper, P.S.,1989

2. Cloning of the essential myotonic dystrophy region and mapping of the putative defect;Aslanidis, C.; Jansen, G.; Amemiya, C.;Nature,1992

3. Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy;Buxton, J.; Shelbourne, P.; Davies, J.;Nature,1992

4. Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy;Harley, H.G.; Brook, J.D.; Rundle, S.A.;Nature,1992

5. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a protein kinase family member;Brook, J.D.; McCurrach, M.E.; Harley, H.G.;Cell,1992

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