Molecular analysis of glycogen storage disease type Ia in Iranian Azeri Turks: identification of a novel mutation.

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Molecular analysis of glycogen storage disease type Ia in Iranian Azeri Turks: identification of a novel mutation.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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Molecular analysis of glycogen ...... ification of a novel mutation.

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Molecular analysis of glycogen ...... ification of a novel mutation.

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Molecular analysis of glycogen ...... ification of a novel mutation.

@en

Molecular analysis of glycogen ...... ification of a novel mutation.

@nl

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Molecular analysis of glycogen ...... ification of a novel mutation.

@en

Molecular analysis of glycogen ...... ification of a novel mutation.

@nl

P1476

Molecular analysis of glycogen ...... ification of a novel mutation.

@en

P2093

Aziz Khorrami

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Mandana Rafeey

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Mansoori Derakhshan Sima

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Robabeh Ghergherehchi

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Shekari Khaniani Mahmoud

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P2860

Glucose-6-phosphatase deficiency

Mutations in the glucose-6-phosphatase gene that cause glycogen storage disease type 1a

Identification of mutations in the gene for glucose-6-phosphatase, the enzyme deficient in glycogen storage disease type 1a

Transmembrane topology of glucose-6-phosphatase

Glycogen storage disease type III diagnosis and management guidelines

Glycogen storage disease type Ia: recent experience with mutation analysis, a summary of mutations reported in the literature and a newly developed diagnostic flow chart.

Glycogen storage diseases: new perspectives.

Mutations in the glucose-6-phosphatase gene are associated with glycogen storage disease types 1a and 1aSP but not 1b and 1c

Molecular genetics of type 1 glycogen storage disease.

Three novel mutations of the G6PC gene identified in Chinese patients with glycogen storage disease type Ia

P2888

s12041-016-0734-y

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19-23

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scholarly article

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10.1007/S12041-016-0734-Y

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P478

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2017-03-01T00:00:00Z

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28360385

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