Diverse driving forces underlie the invariant occurrence of...

Human Molecular Genetics 2008 / 03 Vol. 17; Iss. 13

Diverse driving forces underlie the invariant occurrence of the T42A, E139D, I282V and T468M SHP2 amino acid substitutions causing Noonan and LEOPARD syndromes

Martinelli, S., Torreri, P., Tinti, M., Stella, L., Bocchinfuso, G., Flex, E., Grottesi, A., Ceccarini, M., Palleschi, A., Cesareni, G., Castagnoli, L., Petrucci, T. C., Gelb, B. D., Tartaglia, M.
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Volume:
17
Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/ddn099
Date:
March, 2008
File:
PDF, 669 KB
english, 2008
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