A splice site mutation in the methyltransferase gene FTSJ1 in Xp11.23 is associated with non-syndromic mental retardation in a large Belgian family (MRX9)

Mental retardation is the most frequent cause of serious handicap in children and young adults. The underlying causes of this heterogeneous condition are both acquired and genetically based. A recently performed refinement of the linkage interval in a large Belgian family with mild to severe non-syn...

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Detalhes bibliográficos
Main Authors: Ramser, J, Winnepenninckx, B, Lenski, C, Errijgers, V, Platzer, M, Schwartz, C, Meindl, A, Kooy, R
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 2004
Assuntos:
Short Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1735884/
https://ncbi.nlm.nih.gov/pubmed/15342698
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2004.019000
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