Deleterious mutations in exon 1 of MECP2 in Rett syndrome.
Quenard, Aline
Deleterious mutations in exon 1 of MECP2 in Rett syndrome. [electronic resource] - European journal of medical genetics - 313-22 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1769-7212
10.1016/j.ejmg.2005.11.002 doi
Child, Preschool
Exons--genetics
Female
Humans
Methyl-CpG-Binding Protein 2--genetics
Mutation
Rett Syndrome--genetics
Deleterious mutations in exon 1 of MECP2 in Rett syndrome. [electronic resource] - European journal of medical genetics - 313-22 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1769-7212
10.1016/j.ejmg.2005.11.002 doi
Child, Preschool
Exons--genetics
Female
Humans
Methyl-CpG-Binding Protein 2--genetics
Mutation
Rett Syndrome--genetics