Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: MRAP[original query] |
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Novel polymorphisms and lack of mutations in the ACD gene in patients with ACTH resistance syndromes. Clinical endocrinology 2007 Aug 67 (2): 168-74. Keegan Catherine E, Hutz Janna E, Krause Andrea S, Koehler Katrin, Metherell Louise A, Boikos Sosipatros, Stergiopoulos Sotirios, Clark Adrian J L, Stratakis Constantine A, Huebner Angela, Hammer Gary |
Phenotypic characteristics of familial glucocorticoid deficiency (FGD) type 1 and 2. Clinical endocrinology 2010 May 72 (5): 589-94. Chung Teng-Teng L L, Chan Li F, Metherell Louise A, Clark Adrian J |
Isolated Addison's disease is unlikely to be caused by mutations in MC2R, MRAP or STAR, three genes responsible for familial glucocorticoid deficiency. European journal of endocrinology / European Federation of Endocrine Societies 2010 Feb 162 (2): 357-9. Dias R P, Chan L F, Metherell L A, Pearce S H S, Clark A J |
Determination of alpha-2-MRAP gene polymorphisms in nephrolithiasis patients. International journal of biological macromolecules 2017 Jul . Mehde Atheer Awad, Mehdi Wesen Adel, Yusof Faridah, Raus Raha Ahmed, Abidin Zaima Azira Zainal, Ghazali Hamid, Rahman Azlina A |
Exome-based investigation of the genetic basis of human pigmentary glaucoma. BMC genomics 2021 Jun 22 (1): 477. van der Heide Carly, Goar Wes, Meyer Kacie J, Alward Wallace L M, Boese Erin A, Sears Nathan C, Roos Ben R, Kwon Young H, DeLuca Adam P, Siggs Owen M, Gonzaga-Jauregui Claudia, Sheffield Val C, Wang Kai, Stone Edwin M, Mullins Robert F, Anderson Michael G, Fan Bao Jian, Ritch Robert, Craig Jamie E, Wiggs Janey L, Scheetz Todd E, Fingert John |
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