Síndrome MERRF (Spanish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Síndrome MERRF" in Spanish language version.

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ama-assn.org

Jiménez Escrig, Adriano (2003). Manual de neurogenética. Díaz de Santos. p. 264. ISBN 84-7978-556-X. Consultado el 23 de enero de 2011.

Mancuso M, Filosto M, Mootha VK, et al. (junio de 2004). «A novel mitochondrial tRNAPhe mutation causes MERRF syndrome». Neurology 62 (11): 2119-21. PMID 15184630.

Fukuhara N, Tokiguchi S, Shirakawa K, Tsubaki T (1980). «Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities ): disease entity or a syndrome? Light-and electron-microscopic studies of two cases and review of literature». Journal of the neurological sciences 47 (1). PMID 6774061.
OMIM 545000
Shoffner JM, Wallace DC (1992). «Mitochondrial genetics: principles and practice.». American journal of human genetics 51 (6). PMID 1463005.
Mancuso M, Filosto M, Mootha VK, et al. (junio de 2004). «A novel mitochondrial tRNAPhe mutation causes MERRF syndrome». Neurology 62 (11): 2119-21. PMID 15184630.
Zeviani M, Muntoni F, Savarese N, et al. (1993). «A MERRF/MELAS overlap syndrome associated with a new point mutation in the mitochondrial DNA tRNA(Lys) gene». Eur. J. Hum. Genet. 1 (1): 80-7. PMID 8069654.
Nakamura M, Nakano S, Goto Y, et al. (septiembre de 1995). «A novel point mutation in the mitochondrial tRNA(Ser(UCN)) gene detected in a family with MERRF/MELAS overlap syndrome». Biochem. Biophys. Res. Commun. 214 (1): 86-93. PMID 7669057. doi:10.1006/bbrc.1995.2260.
Melone MA, Tessa A, Petrini S, et al. (febrero de 2004). «Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotype». Arch. Neurol. 61 (2): 269-72. PMID 14967777. doi:10.1001/archneur.61.2.269. (enlace roto disponible en Internet Archive; véase el historial, la primera versión y la última).
Gene reviews - MERRF. Management of patients