Hypoglycaemia revealing heterozygous insulin receptor mutations.

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Hypoglycaemia revealing heterozygous insulin receptor mutations.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年學術文章

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2016年學術文章

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Hypoglycaemia revealing heterozygous insulin receptor mutations.

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Hypoglycaemia revealing heterozygous insulin receptor mutations.

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label

Hypoglycaemia revealing heterozygous insulin receptor mutations.

@en

Hypoglycaemia revealing heterozygous insulin receptor mutations.

@nl

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Hypoglycaemia revealing heterozygous insulin receptor mutations.

@en

Hypoglycaemia revealing heterozygous insulin receptor mutations.

@nl

P1476

Hypoglycaemia revealing heterozygous insulin receptor mutations.

@en

P2093

C Courtillot

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C Feincoeur

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C Vigouroux

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D Maiter

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O Lascols

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P Touraine

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V Preumont

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P2860

A novel syndrome of autosomal-dominant hyperinsulinemic hypoglycemia linked to a mutation in the human insulin receptor gene

Genotype-phenotype correlation in inherited severe insulin resistance.

Autoimmune forms of hypoglycemia.

Substitution of isoleucine for methionine at position 1153 in the beta-subunit of the human insulin receptor. A mutation that impairs receptor tyrosine kinase activity, receptor endocytosis, and insulin action.

Hyperinsulinaemic hypoglycaemia associated with a heterozygous missense mutation of R1174W in the insulin receptor (IR) gene.

Type B Insulin-resistance syndrome: a cause of reversible autoimmune hypoglycaemia.

P304

95-96

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P31

scholarly article

P356

10.1016/J.DIABET.2016.07.001

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P433

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P478

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P577

2016-07-26T00:00:00Z

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P698

27474196

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P921

hypoglycemia

P932

5643506

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