논문KCI 등재
Male hypogonadism caused by a homozygous missense mutation of the LHB gene
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참고문헌 (10)
- Clavijo RI, "Update on male reproductive endocrinology", Transl Androl Urol, 7(Suppl 3), pp.S367~S372 (2018)
- Weiss J, "Hypogonadism caused by a single amino acid substitution in the beta subunit of luteinizing hormone", N Engl J Med, 326, pp.179~183 (1992)
- Lofrano-Porto A, "Luteinizing hormone beta mutation and hypogonadism in men and women", N Engl J Med, 357, pp.897~904 (2007)
- Achard C, "Normal spermatogenesis in a man with mutant luteinizing hormone", N Engl J Med, 361, pp.1856~1863 (2009)
- Potorac I, "A vital region for human glycoprotein hormone trafficking revealed by an LHB mutation", J Endocrinol, 231, pp.197~207 (2016)
- Yang X, "Homozygous nonsense mutation Trp28X in the LHB gene causes male hypogonadism", J Assist Reprod Genet, 35, pp.913~919 (2018)
- Valdes-Socin H, "Hypogonadism in a patient with a mutation in the luteinizing hormone beta-subunit gene", N Engl J Med, 351, pp.2619~2625 (2004)
- Basciani S, "Hypogonadism in a patient with two novel mutations of the luteinizing hormone β-subunit gene expressed in a compound heterozygous form", J Clin Endocrinol Metab, 97, pp.3031~3038 (2012)
- Jae Won Song, "Hypogonadotrophic hypogonadism due to a mutation in the luteinizing hormone β-subunit gene", The Korean Journal of Internal Medicine, 33(3), pp.638~641 (2018), 대한내과학회[DOI]
- Hernan Valdes-Socin, "Comment on “Hypogonadotrophic hypogonadism due to a mutation in the luteinizing hormone β-subunit gene”", The Korean Journal of Internal Medicine, 32(3), pp.566~567 (2017), 대한내과학회[DOI]
관련 논문AI추천
Hypogonadotrophic hypogonadism due to a mutation in the luteinizing hormone β-subunit gene김철식, 이성진, Chang Min Lee, Gun Ha Park, Hyo-Jeong Hwang, Jae Won Song, Sung-Hee Ihm대한내과학회 · The Korean Journal of Internal Medicine2018 · 제33권 제3호Comment on “Hypogonadotrophic hypogonadism due to a mutation in the luteinizing hormone β-subunit gene”Adrian F. Daly, Albert Beckers, Hernan Valdes-Socin대한내과학회 · The Korean Journal of Internal Medicine2017 · 제32권 제3호Response to comment on “Hypogonadotrophic hypogonadism due to a mutation in the luteinizing hormone β-subunit gene”임성희대한내과학회 · The Korean Journal of Internal Medicine2017 · 제32권 제3호A novel compound variant in GNRHR causing congenital idiopathic hypogonadotropic hypogonadism in a young male Korean patientLee Gimin, Lee Mi-Seon, Lee Rosie, Moon Jung-EunA novel variant in NR0B1 causing X-linked adrenal hypoplasia congenitaHeo Seung, Hwang Jin Soon, Lee Hae Sang, Shim Young Suk대한소아내분비학회 · Annals of Pediatric Endocrinology & Metabolism2024 · 제29권 제3호Identification of a novel mutation of the SHOX gene in a patient with Leri-Weill dyschondrosteosis accompanied by growth hormone deficiency전종근, Kang Jaebeen, Kim Min-Ji, Yoo Sukdong대한소아내분비학회 · Annals of Pediatric Endocrinology & Metabolism2024 · 제29권 제3호
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