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Mutations in the translated region of the lactase gene (LCT) underlie congenital lactase deficiency.
Am J Hum Genet. 2006 Feb;78(2):339-44. doi: 10.1086/500053. Epub 2005 Dec 15.
Am J Hum Genet. 2006.
PMID: 16400612
Free PMC article.
Molecularly defined adult-type hypolactasia among working age people with reference to milk consumption and gastrointestinal symptoms.
Anthoni SR, Rasinperä HA, Kotamies AJ, Komu HA, Pihlajamäki HK, Kolho KL, Järvelä IE.
Anthoni SR, et al. Among authors: komu ha.
World J Gastroenterol. 2007 Feb 28;13(8):1230-5. doi: 10.3748/wjg.v13.i8.1230.
World J Gastroenterol. 2007.
PMID: 17451204
Free PMC article.
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Screening of mutations in the PHF8 gene and identification of a novel mutation in a Finnish family with XLMR and cleft lip/cleft palate.
Koivisto AM, Ala-Mello S, Lemmelä S, Komu HA, Rautio J, Järvelä I.
Koivisto AM, et al. Among authors: komu ha.
Clin Genet. 2007 Aug;72(2):145-9. doi: 10.1111/j.1399-0004.2007.00836.x.
Clin Genet. 2007.
PMID: 17661819
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Lactase non-persistence and milk consumption in Estonia.
Lember M, Torniainen S, Kull M, Kallikorm R, Saadla P, Rajasalu T, Komu H, Järvelä I.
Lember M, et al. Among authors: komu h.
World J Gastroenterol. 2006 Dec 7;12(45):7329-31. doi: 10.3748/wjg.v12.i45.7329.
World J Gastroenterol. 2006.
PMID: 17143950
Free PMC article.
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Linkage and candidate gene studies of autism spectrum disorders in European populations.
Holt R, Barnby G, Maestrini E, Bacchelli E, Brocklebank D, Sousa I, Mulder EJ, Kantojärvi K, Järvelä I, Klauck SM, Poustka F, Bailey AJ, Monaco AP; EU Autism MOLGEN Consortium.
Holt R, et al.
Eur J Hum Genet. 2010 Sep;18(9):1013-9. doi: 10.1038/ejhg.2010.69. Epub 2010 May 5.
Eur J Hum Genet. 2010.
PMID: 20442744
Free PMC article.
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