Literature DB >> 21488243

Novel human pathological mutations. Gene symbol: MC2R. Disease: glucocorticoid deficiency.

O Thomas Mueller1, A Coovadia.   

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Year:  2010        PMID: 21488243

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


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  1 in total

1.  The Genetic Perspective of Familial Glucocorticoid Deficiency: In Silico Analysis of Two Novel Variants.

Authors:  Katayoun Heshmatzad; Nejat Mahdieh; Ali Rabbani; Abdolah Didban; Bahareh Rabbani
Journal:  Int J Endocrinol       Date:  2020-09-01       Impact factor: 3.257

  1 in total

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