MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin. [electronic resource]
Producer: 20010607Description: 1093-101 p. digitalISSN:- 0002-9297
- Adult
- Alleles
- Base Sequence
- Chromosomal Proteins, Non-Histone
- DNA Mutational Analysis
- DNA-Binding Proteins -- genetics
- Female
- Gene Frequency -- genetics
- Genetic Counseling
- Genetic Linkage -- genetics
- Genetic Predisposition to Disease
- Genotype
- Humans
- Introns -- genetics
- Male
- Maternal Age
- Methyl-CpG-Binding Protein 2
- Molecular Sequence Data
- Mutation -- genetics
- Paternal Age
- Point Mutation -- genetics
- Polymorphism, Single Nucleotide -- genetics
- Repressor Proteins
- Rett Syndrome -- genetics
- Sequence Deletion -- genetics
- Sex Distribution
- X Chromosome -- genetics
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Publication Type: Journal Article
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