Lost in translation: translational interference from a recurrent mutation in exon 1 of MECP2
Background: Rett syndrome (RTT) is an X linked neuro-developmental disorder affecting
mostly girls. Mutations in the coding region of MECP2 are found in 80% of classic RTT …
mostly girls. Mutations in the coding region of MECP2 are found in 80% of classic RTT …
[PDF][PDF] Lost in translation: translational interference from
…, P MacLeod, D Ravine, A Saxena, D de Lagarde… - J Med Genet, 2006 - Citeseer
Background: Rett syndrome (RTT) is an X linked neuro-developmental disorder affecting
mostly girls. Mutations in the coding region of MECP2 are found in 80% of classic RTT …
mostly girls. Mutations in the coding region of MECP2 are found in 80% of classic RTT …
[CITATION][C] La formación de la sociedad colonial más peculiar del Imperio español: la emigración europea a Filipinas en la primera mitad del siglo XVII
AD LAGARDE - 2008 - PhD Dissertation, Universidad …
[CITATION][C] El aspecto político del proceso inquisitorial contra Fray Jorge de Santa María seguido en Manila entre 1659-1661
AD de Lagarde - 1996 - Facultad de Filosofía y Letras …