Trappe, R <br/><br/>
MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin.  [electronic resource] 

 -  American journal of human genetics  May 2001 
 - 1093-101 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0002-9297 
<br/><br/><label>Standard No.: </label>10.1086/320109  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Alleles<br/>Base Sequence<br/>Chromosomal Proteins, Non-Histone<br/>DNA Mutational Analysis<br/>DNA-Binding Proteins--genetics<br/>Female<br/>Gene Frequency--genetics<br/>Genetic Counseling<br/>Genetic Linkage--genetics<br/>Genetic Predisposition to Disease<br/>Genotype<br/>Humans<br/>Introns--genetics<br/>Male<br/>Maternal Age<br/>Methyl-CpG-Binding Protein 2<br/>Molecular Sequence Data<br/>Mutation--genetics<br/>Paternal Age<br/>Point Mutation--genetics<br/>Polymorphism, Single Nucleotide--genetics<br/>Repressor Proteins<br/>Rett Syndrome--genetics<br/>Sequence Deletion--genetics<br/>Sex Distribution<br/>X Chromosome--genetics