抽象的

Mutational Investigations in PIT Genes

Jhansi Rani K

In the present study, we performed mutational investigation of the PIT1 qualities in a partner of 40 patients with idiopathic hypopituitarism followed in one substantial neuroendocrinology Hospital, Guntur, Andhra Pradesh, India. Since LHX4 and HESX1 are more prone to be connected with EPP, and LHX3, PIT1, PROP1, and HESX1 with NPPP, We have broke down the Pit-1 succession of three obviously autonomous families in which hypopituitary kids are homozygous and phenotypically typical folks are heterozygous for a Pro239Ser change

索引于

化学文摘社 (CAS)
哥白尼索引
打开 J 门
学术钥匙
研究圣经
引用因子
电子期刊图书馆
参考搜索
哈姆达大学
学者指导
国际创新期刊影响因子(IIJIF)
国际组织研究所 (I2OR)
宇宙
日内瓦医学教育与研究基金会
秘密搜索引擎实验室

查看更多