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The most recurrent monogenic disorders that overlap with the phenotype of Rett syndrome
by
Vidal, S.
,
Brandi, N.
,
Pacheco, P.
,
Maynou, J.
,
Fernandez, G.
,
Xiol, C.
,
Pascual-Alonso, A.
,
Pineda, M.
,
Maria del Mar, O'Callaghan
,
Garcia-Cazorla, Àngels
,
del Carmen Serrano Munuera, Maria
,
García, Silvia Cuso
,
Troncoso, Monica
,
Fariña, Guillermo
,
García Peñas, Juan José
,
Fournier, Belen Gil
,
León, Soraya Ramiro
,
Guitart, Miriam
,
Baena, Neus
,
de Nanclares, Guiomar Perez
,
Oci, Intzane Ocio
,
Gutiérrez-Delicado, Eva
,
Abarrategui, Belén
,
Barroso, Eva
,
Santos-Simarro, Fernando
,
Lapunzina, Pablo
,
García, Francisco J.
,
Acedo, Juan M.
,
García, Asunción
,
Martinez, Miguel A.
,
Martínez-Bermejo, Antonio
,
Armstrong, J.
Published in
European journal of paediatric neurology
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European Journal Of Paediatric Neurology
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Clinical Neurology
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Genotype-Phenotype Correlations
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Life Sciences & Biomedicine
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Mecp2
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Monogenic Disorders
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Neurosciences & Neurology
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Pediatrics
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Rett Syndrome
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Rett-Like
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Rtt
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