Case Report
A Novel RET D898Y Germline Mutation in a Patient with Pheochromocytoma
Table 1
Paraganglioma/pheochromocytoma genetic mutational panel screened in the rare disease control program in Korea.
| Gene | Reference sequence |
| MAX | NG_029830.1, NM_002382.4 | NF1 | NG_009018.1, NM_000267.3 | RET | NG_007489.1, NM_020975.4 | SDHA | NG_012339.1, NM_004168.2 | SDHAF2 | NG_023393.1, NM_017841.2 | SDHB | NG_012340.1, NM_003000.2 | SDHC | NG_012767.1, NM_003001.3 | SDHD | NG_012337.2, NM_003002.2 | TMEM127 | NG_027695.1, NM_017849.3 | VHL | NG_008212.3, NM_000551.3 |
|
|