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Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood
Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood
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Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood

Edghill, Emma L ; Flanagan, Sarah E ; Patch, Ann-Marie ; Boustred, Chris ; Parrish, Andrew ; Shields, Beverley ; Shepherd, Maggie H ; Hussain, Khalid ; Kapoor, Ritika R ; Malecki, Maciej ; MacDonald, Michael J ; Støy, Julie ; Steiner, Donald F ; Philipson, Louis H ; Bell, Graeme I ; Hattersley, Andrew T ; Ellard, Sian

Diabetes (New York, N.Y.), 2008-04, Vol.57 (4), p.1034 [Periódico revisado por pares]

United States: American Diabetes Association

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Insulin Mutation Screening in 1,044 Patients With Diabetes
Insulin Mutation Screening in 1,044 Patients With Diabetes
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Insulin Mutation Screening in 1,044 Patients With Diabetes

Edghill, Emma L. ; Flanagan, Sarah E. ; Patch, Ann-Marie ; Boustred, Chris ; Parrish, Andrew ; Shields, Beverley ; Shepherd, Maggie H. ; Hussain, Khalid ; Kapoor, Ritika R. ; Malecki, Maciej ; MacDonald, Michael J. ; Støy, Julie ; Steiner, Donald F. ; Philipson, Louis H. ; Bell, Graeme I. ; Hattersley, Andrew T. ; Ellard, Sian

Diabetes (New York, N.Y.), 2008-04, Vol.57 (4), p.1034-1042 [Periódico revisado por pares]

American Diabetes Association

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Insulin Mutation Screening in 1,044 Patients With Diabetes : Mutations in the INS Gene Are a Common Cause of Neonatal Diabetes but a Rare Cause of Diabetes Diagnosed in Childhood or Adulthood. Commentary
Insulin Mutation Screening in 1,044 Patients With Diabetes : Mutations in the INS Gene Are a Common Cause of Neonatal Diabetes but a Rare Cause of Diabetes Diagnosed in Childhood or Adulthood. Commentary
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Insulin Mutation Screening in 1,044 Patients With Diabetes : Mutations in the INS Gene Are a Common Cause of Neonatal Diabetes but a Rare Cause of Diabetes Diagnosed in Childhood or Adulthood. Commentary

GLASER, Benjamin ; EDGHILL, Emma L ; MALECKI, Maciej ; MACDONALD, Michael J ; STØY, Julie ; STEINER, Donald F ; PHILIPSON, Louis H ; BELL, Graeme I ; HATTERSLEY, Andrew T ; ELLARD, Sian ; FLANAGAN, Sarah E ; PATCH, Ann-Marie ; BOUSTRED, Chris ; PARRISH, Andrew ; SHIELDS, Beverley ; SHEPHERD, Maggie H ; HUSSAIN, Khalid ; KAPOOR, Ritika R

Diabetes (New York, N.Y.), 2008, Vol.57 (4) [Periódico revisado por pares]

Alexandria, VA: American Diabetes Association

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Insulin Mutation Screening in 1044 Patients with Diabetes: Mutations in the INS gene are a Common Cause of Neonatal Diabetes but a Rare Cause of Diabetes Diagnosed in Childhood or Adulthood
Insulin Mutation Screening in 1044 Patients with Diabetes: Mutations in the INS gene are a Common Cause of Neonatal Diabetes but a Rare Cause of Diabetes Diagnosed in Childhood or Adulthood
Material Type:
Artigo 		Adicionar ao Meu Espaço

Insulin Mutation Screening in 1044 Patients with Diabetes: Mutations in the INS gene are a Common Cause of Neonatal Diabetes but a Rare Cause of Diabetes Diagnosed in Childhood or Adulthood

Edghill, Emma L. ; Flanagan, Sarah E. ; Patch, Ann-Marie ; Boustred, Chris ; Parrish, Andrew ; Shields, Beverley ; Shepherd, Maggie H. ; Hussain, Khalid ; Kapoor, Ritika R. ; Malecki, Maciej ; MacDonald, Michael J. ; Støy, Julie ; Steiner, Donald F. ; Philipson, Louis H. ; Bell, Graeme I. ; Hattersley, Andrew T. ; Ellard, Sian

Diabetes (New York, N.Y.), 2007-12, Vol.57 (4), p.1034-42 [Periódico revisado por pares]

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