Cognitive profile in childhood myotonic dystrophy type 1: Is there a global impairment?

Author:

Angeard Nathalie,Gargiulo Marcela,Jacquette Aurélia,Radvanyi Hélène,Eymard Bruno,Héron Delphine

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference45 articles.

1. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3’ end of a transcript encoding a protein kinase family member;Brook;Cell,1992

2. An unstable triplet repeat in a gene related to myotonic muscular dystrophy;Fu;Science,1992

3. Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy;Harley;Am J Hum Gen,1993

4. Genetic risks for children of women with myotonic dystrophy;Koch;Am J Hum Genet,1991

5. de Die-Smulders C. Congenital and childhood-onset myotonic dystrophy. In: Harper PS, van Engelen B, Eymard B, Wilcox, DE editors. Myotonic dystrophy: present management, future therapy, Oxford University: 2004. p. 162–75.

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