Biochemical and Structural characterization of Noonan syndrome-causing mutations affecting SHP-2’s phoshotyrosyl-binding pockets

Authors :: Martinelli, S
Torreri, P
Bocchinfuso, G
Stella, L
Flex, E
Grottesi, A
Chillemi, G
Ceccarini, M
Palleschi, A
Gelb, B
Petrucci, T
Tartaglia, M
Publication Year :: 2007
Publisher :: European Society of Human Genetics, 2007.

Subjects :: SHP-2
Noonan syndrome, PTPN11, SHP-2
Noonan syndrome
PTPN11
Settore CHIM/02 - Chimica Fisica

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