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ptpn11 protein, human
(compound)
Summary
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Genetic Markers
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No genes found
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No biogroups found
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Most Correlated Studies
Melanoma patient derived xenograft (PDX) and WM3248 cells treated with ARN22089
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Literature
Most Relevant Literature
Phacomatosis pigmentovascularis spilorosea and mutation in the PTPN11 gene: new case with significan…
PTPN11 Mosaicism Causes a Spectrum of Pigmentary and Vascular Neurocutaneous Disorders and Predispos…
The clinical phenotype and gene analysis of syndromic deafness with PTPN11 gene mutation].
Transient abnormal lymphomyelopoiesis in a newborn with PTPN11 mutation associated Noonan syndrome.
A preterm newborn-onset juvenile myelomonocytic leukemia-like myeloproliferation with PTPN11 mutatio…
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A Study of PEG-somatropin in the Treatment of Children With Idiopathic Short Stature
Treatment With HMG-COA Reductase Inhibitor of Growth and Bone Abnormalities in Children With Noonan …
Vinblastine +/- Bevacizumab in Children With Unresectable or Progressive Low Grade Glioma (LGG)
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