Literature DB >> 35635658

Heterozygous POR gene mutations in a patient with congenital adrenal hyperplasia.

Carmelo Gusmano1, Aldo E Calogero2, Rossella Cannarella1.   

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Year:  2022        PMID： 35635658     DOI： 10.1007/s12020-022-03086-9

Source DB:  PubMed          Journal:  Endocrine        ISSN： 1355-008X            Impact factor:   3.925


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  1 in total

1.  Genetic aetiology of primary adrenal insufficiency in Chinese children.

Authors:  Zhuo Chang; Wei Lu; Zhuhui Zhao; Li Xi; Xiaojing Li; Rong Ye; Jinwen Ni; Zhou Pei; Miaoying Zhang; Ruoqian Cheng; Zhangqian Zheng; Chengjun Sun; Jing Wu; Feihong Luo
Journal:  BMC Med Genomics       Date:  2021-06-30       Impact factor: 3.063
  1 in total

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