Mutational analysis of SHOC2, a novel gene for Noonan-like syndrome, in JMML
Copyright policy )Mutational analysis of SHOC2, a novel gene for Noonan-like syndrome, in JMML
To the editor: Cordeddu et al recently reported the discovery of a specific SHOC2 gene mutation underlying a variant of the neuro-cardio-facio-cutaneous (NCFC) syndrome family.[1][1] The common denominator of mutations associated with this group of disorders is their involvement in the
- University of Freiburg Germany
- Boston Children's Hospital United States
- Erasmus University Medical Center Netherlands
- University of Zurich Switzerland
- University Children's Hospital Zurich Switzerland
2403 Immunology, 1303 Biochemistry, MAP Kinase Signaling System, 2720 Hematology, DNA Mutational Analysis, Noonan Syndrome, Intracellular Signaling Peptides and Proteins, 610 Medicine & health, EMC MM-02-54-03, 1307 Cell Biology, Leukemia, Myelomonocytic, Juvenile, 10036 Medical Clinic, Humans
2403 Immunology, 1303 Biochemistry, MAP Kinase Signaling System, 2720 Hematology, DNA Mutational Analysis, Noonan Syndrome, Intracellular Signaling Peptides and Proteins, 610 Medicine & health, EMC MM-02-54-03, 1307 Cell Biology, Leukemia, Myelomonocytic, Juvenile, 10036 Medical Clinic, Humans
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