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Published in 2024 at "Frontiers in Oncology"
DOI: 10.3389/fonc.2024.1451576
Abstract: Objective This study focused on the analysis of the correlation between common gene mutation types and metastatic sites in NSCLC patients. Methods We retrospectively studied 1586 NSCLC patients and used fluorescence Polymerase chain reaction (PCR)…
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Keywords:
lung;
mutation group;
metastasis patients;
mutation ... See more keywords
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Published in 2021 at "Frontiers in Pediatrics"
DOI: 10.3389/fped.2021.699767
Abstract: Background: X-linked hypophosphatemia (XLH) is the most frequent form of hypophosphatemic rickets and is caused by mutations in the PHEX gene. We analyzed genotype-phenotype correlations in XLH patients with proven PHEX mutations. Methods: PHEX mutations…
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Keywords:
genotype phenotype;
truncating mutation;
linked hypophosphatemia;
mutation group ... See more keywords