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Diabetes mellitus (hereditary)
LE WE PMID CA
Diabetes mellitus (hereditary)673Diabetes mellitus (Hereditaer)

ABCC8 SUR1

Anemia (megaloblastic thiamine responsive)

Bererdinelli Seip congenital lipodystrophy

BSCL1 AGPAT2

BSCL2 Seipin

Diabetes mellitus (Hereditary MODY)

Diabetes mellitus (hereditary)

Diabetes mellitus (neonatal)

Donohue s syndrome Leprechaunism

EIF2AK3 PERK

FRDA1 Frataxin

Friedreich ataxia

GADD153 CHOP

Glucokinase

GLUD1

Insulin (Biosynthesis and Regulation)

Insulin resistance type a

KCNJ11 Kir6 2

Lipodystrophy

OMIM_601487

OMIM_x600937

Persistent hyperinsulinemic hypoglycemia of infancy

Persistent neonatal hypoglycemia

Rabson Mendenhall s syndrome

Receptor (Insulin)

Receptor (PPAR gamma)

SLC19A2 THTR1

TNDM29locus

Werner s syndrome

Wfs1 Wolframin

Wfs2

Wolcott Rallison syndrome

Wolfram s syndrome DIDMOAD

WRN

1999  
1
Genetically defined forms of diabetes in children.
[10599693] J Clin Endocrinol Metab 84(12): 4390-6 (1999)
2008  
2
Monogenic diabetes in the young, pharmacogenetics and relevance to multifactorial forms of type 2 diabetes.
[18436708] Endocr Rev 29(3): 254-64 (2008)
2010  
3
2010  
4
In vitro processing and secretion of mutant insulin proteins that cause permanent neonatal diabetes.
[19952343] Am J Physiol Endocrinol Metab 298(3): E403-10 (2010)
2006  
5
Monogenic diabetes in children and young adults: Challenges for researcher, clinician and patient.
[17186387] Rev Endocr Metab Disord 7(3): 171-85 (2006)
2005  
6
Monogenic syndromes of abnormal glucose homeostasis: clinical review and relevance to the understanding of the pathology of insulin resistance and beta cell failure.
[15772126] J Med Genet 42(12): 893-902 (2005)

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All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.


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