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Heterogeneity of vitamin D receptor gene association with celiac disease and type 1 diabetes mellitus.
Autoimmunity. 2005 Sep;38(6):439-44. doi: 10.1080/08916930500288455.
Autoimmunity. 2005.
PMID: 16278149
Free article.
Mutations in GCK and HNF-1alpha explain the majority of cases with clinical diagnosis of MODY in Spain.
Estalella I, Rica I, Perez de Nanclares G, Bilbao JR, Vazquez JA, San Pedro JI, Busturia MA, Castaño L; Spanish MODY Group.
Estalella I, et al. Among authors: san pedro ji.
Clin Endocrinol (Oxf). 2007 Oct;67(4):538-46. doi: 10.1111/j.1365-2265.2007.02921.x. Epub 2007 Jun 15.
Clin Endocrinol (Oxf). 2007.
PMID: 17573900
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Haploinsufficiency at GCK gene is not a frequent event in MODY2 patients.
Garin I, Rica I, Estalella I, Oyarzabal M, Rodríguez-Rigual M, San Pedro JI, Pérez-Nanclares G, Fernández-Rebollo E, Busturia MA, Castaño L, Pérez de Nanclares G; Spanish MODY Group.
Garin I, et al. Among authors: san pedro ji.
Clin Endocrinol (Oxf). 2008 Jun;68(6):873-8. doi: 10.1111/j.1365-2265.2008.03214.x. Epub 2008 Feb 1.
Clin Endocrinol (Oxf). 2008.
PMID: 18248649
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