Literature DB >> 17371482

Congenital adrenal hyperplasia in a Nigerian child with a novel compound heterozygote mutation in CYP11B1.

M Andrew, M Barr, E Davies, A M Wallace, J M Connell, S F Ahmed.   

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Year:  2007        PMID： 17371482     DOI： 10.1111/j.1365-2265.2007.02766.x

Source DB:  PubMed          Journal:  Clin Endocrinol (Oxf)        ISSN： 0300-0664            Impact factor:   3.478


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  3 in total

Review 1.  Congenital Micropenis: Etiology And Management.

Authors:  Marianna Rita Stancampiano; Kentaro Suzuki; Stuart O'Toole; Gianni Russo; Gen Yamada; Syed Faisal Ahmed
Journal:  J Endocr Soc       Date:  2021-11-15

2.  Functional consequences of seven novel mutations in the CYP11B1 gene: four mutations associated with nonclassic and three mutations causing classic 11{beta}-hydroxylase deficiency.

Authors:  Silvia Parajes; Lourdes Loidi; Nicole Reisch; Vivek Dhir; Ian T Rose; Rainer Hampel; Marcus Quinkler; Gerard S Conway; Lidia Castro-Feijóo; David Araujo-Vilar; Manuel Pombo; Fernando Dominguez; Emma L Williams; Trevor R Cole; Jeremy M Kirk; Elke Kaminsky; Gill Rumsby; Wiebke Arlt; Nils Krone
Journal:  J Clin Endocrinol Metab       Date:  2010-01-20       Impact factor: 5.958

Review 3.  Non-classical 11β-hydroxylase deficiency caused by compound heterozygous mutations: a case study and literature review.

Authors:  Dongdong Wang; Jiahui Wang; Tong Tong; Qing Yang
Journal:  J Ovarian Res       Date:  2018-09-17       Impact factor: 4.234
  3 in total

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