The RET C620S mutation causes multiple endocrine neoplasia type 2A (MEN2A) but not Hirschsprung disease (HSCR) in a family cosegregating both phenotypes?

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DOI:10.1002/humu.10273
作者：Raquel M. Fernández, Guillermo Anti?olo, Charis Eng, Salud Borrego
文献类型：期刊论文
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文献链接：https://doi.org/10.1002/humu.10273

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Abstract：The RET proto-oncogene (MIM# 164761), located on chromosome subband 10q11.2, encodes a receptor tyrosine kinase expressed in tissues and tumors derived from the neural crest. The ligands of

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上一个求助:其它数据库Naturally Fractured Carbonate Reservoir Characterization: A Case Study of a Mature High-Pour Point Oil Field in Hungary 下一个求助:Thieme Medical PublishersWithin-gene interaction between c.135 G/A genotypes and RET proto-oncogene germline mutations in HSCR families.