MECP2 Mutations in Sporadic Cases of Rett Syndrome Are Almost Exclusively of Paternal Origin - Concepedia

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MECP2 Mutations in Sporadic Cases of Rett Syndrome Are Almost Exclusively of Paternal Origin

DOI Full Paper Access

282

Citations

26

References

2001

Year

Ralf Ulrich Trappe, Franco Laccone, Joana Cobilanschi, Moritz Meins, Peter Huppke, F. Hanefeld, Wolfgang Engel

The American Journal of Human Genetics

Mendelian DisorderGenetic DisorderGeneticsMecp2 MutationsPathologyMolecular GeneticsChromosomal RearrangementPaternal OriginMedicineSporadic CasesClinical Genetics

References

	Year	Citations

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