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Results 1 - 10 of 11 for korean disease
  1. Caffey disease 
    ... 3040C > T mutation in COL1A1 is recurrent in Korean patients with infantile cortical hyperostosis (Caffey disease). J Hum Genet. 2008;53(10):947. doi: ...
    https://medlineplus.gov/genetics/condition/caffey-disease - Genetics
  2. COQ2 gene 
    ... and multiple system atrophy in other populations, including Koreans, Europeans, and North Americans. It remains unclear whether COQ2 gene variations represent a significant risk factor for this disease.Researchers speculate that changes in the COQ2 gene ...
    https://medlineplus.gov/genetics/gene/coq2 - Genetics
  3. HLA-DQB1 gene 
    ... 0301 and DQB1*0601 modulate narcolepsy susceptibility in Koreans. Hum Immunol. ... II proteins and disease: a structural perspective. Nat Rev Immunol. 2006 Apr; ...
    https://medlineplus.gov/genetics/gene/hla-dqb1 - Genetics
  4. Heterotaxy syndrome 
    ... S1047951107001138. Citation on PubMed Kim SJ. Heterotaxy syndrome. ... for heart disease associated with abnormal sidedness. Teratology. 2002 Nov;66( ...
    https://medlineplus.gov/genetics/condition/heterotaxy-syndrome - Genetics
  5. SNCA gene 
    ... Variations in the SNCA gene appear to affect disease risk in people of European descent; however, studies suggest that changes in this gene are not associated with multiple system atrophy in the Chinese population or in South Koreans. It is unclear whether SNCA gene variations are ...
    https://medlineplus.gov/genetics/gene/snca - Genetics
  6. Beare-Stevenson cutis gyrata syndrome 
    ... FGF signaling in skeletal development and human genetic diseases. Front Biosci. 2005 May 1;10:1961-76. doi: 10.2741/1671. Citation on PubMed Eun SH, Ha KS, Je BK, Lee ES, Choi BM, Lee JH, Eun BL, Yoo KH. The first Korean case of Beare-Stevenson syndrome with a Tyr375Cys ...
    https://medlineplus.gov/.../beare-stevenson-cutis-gyrata-syndrome - Genetics
  7. Palmoplantar keratoderma with deafness 
    ... TW. Connexin-26 mutations in deafness and skin disease. Expert Rev Mol Med. 2009 ... genetic mutation of Connexin 26. J Korean Med Sci. 2010 Oct;25(10):1539-42. ...
    https://medlineplus.gov/.../palmoplantar-keratoderma-with-deafness - Genetics
  8. Progressive familial heart block 
    ... Progressive familial heart block type I in a korean patient. Korean Circ J. 2011 May;41(5):276-9. ... mutations associated with Brugada syndrome and cardiac conduction disease in humans. J Clin Invest. 2008 Jun;118( ...
    https://medlineplus.gov/.../progressive-familial-heart-block - Genetics
  9. Gestational diabetes 
    ... wide association study of gestational diabetes mellitus in Korean women. Diabetes. 2012 Feb;61(2):531-41. ...
    https://medlineplus.gov/genetics/condition/gestational-diabetes - Genetics
  10. Fibromyalgia 
    ... SS. New insights into the genetics of fibromyalgia. Korean J Intern Med. 2017 Nov;32(6):984- ...
    https://medlineplus.gov/genetics/condition/fibromyalgia - Genetics
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