Functional and cellular characterization of human Retinoic Acid Induced 1 (RAI1) mutations associated with Smith-Magenis Syndrome

Carmona-Mora, P; Encina, C.A; Canales, CP; Cao, L.; Molina, J; Kairath P.; Walz, K

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Título según WOS: Functional and cellular characterization of human Retinoic Acid Induced 1 (RAI1) mutations associated with Smith-Magenis Syndrome
Título según SCOPUS: Functional and cellular characterization of human Retinoic Acid Induced 1 (RAI1) mutations associated with Smith-Magenis Syndrome
Título de la Revista: BMC Molecular Biology
Volumen: 11
Editorial: Springer Nature
Fecha de publicación: 2010
Idioma: English
URL: http://www.biomedcentral.com/1471-2199/11/63
DOI:

10.1186/1471-2199-11-63

Notas: ISI, SCOPUS