Erratum: Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome (Nature Genetics DOI: 10.1038/ng1939)

Marco Tartaglia; Len A. Pennacchio; Chen Zhao; Kamlesh K. Yadav; Valentina Fodale; Anna Sarkozy; Bhaswati Pandit; Kimihiko Oishi; Simone Martinelli; Wendy Schackwitz; Anna Ustaszewska; Joel Martin; James Bristow; Claudio Carta; Francesca Lepri; Cinzia Neri; Isabella Vasta; Kate Gibson; Cynthia J. Curry; Juan Pedro López Siguero; Maria Cristina Digilio; Giuseppe Zampino; Bruno Dallapiccola; Dafna Bar-Sagi; Bruce D. Gelb

doi:10.1038/ng0207-276a

Erratum: Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome (Nature Genetics DOI: 10.1038/ng1939)

Marco Tartaglia, Len A. Pennacchio, Chen Zhao, Kamlesh K. Yadav, Valentina Fodale, Anna Sarkozy, Bhaswati Pandit, Kimihiko Oishi, Simone Martinelli, Wendy Schackwitz, Anna Ustaszewska, Joel Martin, James Bristow, Claudio Carta, Francesca Lepri, Cinzia Neri, Isabella Vasta, Kate Gibson, Cynthia J. Curry, Juan Pedro López SigueroMaria Cristina Digilio, Giuseppe Zampino, Bruno Dallapiccola, Dafna Bar-Sagi, Bruce D. Gelb

Research output: Contribution to journal › Comment/debate

3 Scopus citations

Original language	English
Pages (from-to)	276
Number of pages	1
Journal	Nature Genetics
Volume	39
Issue number	2
DOIs	https://doi.org/10.1038/ng0207-276a
State	Published - Feb 2007

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10.1038/ng0207-276a

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Tartaglia, M., Pennacchio, L. A., Zhao, C., Yadav, K. K., Fodale, V., Sarkozy, A., Pandit, B., Oishi, K., Martinelli, S., Schackwitz, W., Ustaszewska, A., Martin, J., Bristow, J., Carta, C., Lepri, F., Neri, C., Vasta, I., Gibson, K., Curry, C. J., ... Gelb, B. D. (2007). Erratum: Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome (Nature Genetics DOI: 10.1038/ng1939). Nature Genetics, 39(2), 276. https://doi.org/10.1038/ng0207-276a

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author = "Marco Tartaglia and Pennacchio, {Len A.} and Chen Zhao and Yadav, {Kamlesh K.} and Valentina Fodale and Anna Sarkozy and Bhaswati Pandit and Kimihiko Oishi and Simone Martinelli and Wendy Schackwitz and Anna Ustaszewska and Joel Martin and James Bristow and Claudio Carta and Francesca Lepri and Cinzia Neri and Isabella Vasta and Kate Gibson and Curry, {Cynthia J.} and Siguero, {Juan Pedro L{\'o}pez} and Digilio, {Maria Cristina} and Giuseppe Zampino and Bruno Dallapiccola and Dafna Bar-Sagi and Gelb, {Bruce D.}",

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Tartaglia, M, Pennacchio, LA, Zhao, C, Yadav, KK, Fodale, V, Sarkozy, A, Pandit, B, Oishi, K, Martinelli, S, Schackwitz, W, Ustaszewska, A, Martin, J, Bristow, J, Carta, C, Lepri, F, Neri, C, Vasta, I, Gibson, K, Curry, CJ, Siguero, JPL, Digilio, MC, Zampino, G, Dallapiccola, B, Bar-Sagi, D & Gelb, BD 2007, 'Erratum: Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome (Nature Genetics DOI: 10.1038/ng1939)', Nature Genetics, vol. 39, no. 2, pp. 276. https://doi.org/10.1038/ng0207-276a

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AU - Pennacchio, Len A.

AU - Zhao, Chen

AU - Yadav, Kamlesh K.

AU - Fodale, Valentina

AU - Sarkozy, Anna

AU - Pandit, Bhaswati

AU - Oishi, Kimihiko

AU - Martinelli, Simone

AU - Schackwitz, Wendy

AU - Ustaszewska, Anna

AU - Martin, Joel

AU - Bristow, James

AU - Carta, Claudio

AU - Lepri, Francesca

AU - Neri, Cinzia

AU - Vasta, Isabella

AU - Gibson, Kate

AU - Curry, Cynthia J.

AU - Siguero, Juan Pedro López

AU - Digilio, Maria Cristina

AU - Zampino, Giuseppe

AU - Dallapiccola, Bruno

AU - Bar-Sagi, Dafna

AU - Gelb, Bruce D.

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