Polycystic ovary syndrome in mitochondrial disorders due mtDNA or nDNA variants.

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Polycystic ovary syndrome in mitochondrial disorders due mtDNA or nDNA variants.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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Polycystic ovary syndrome in mitochondrial disorders due mtDNA or nDNA variants.

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Polycystic ovary syndrome in mitochondrial disorders due mtDNA or nDNA variants.

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label

Polycystic ovary syndrome in mitochondrial disorders due mtDNA or nDNA variants.

@en

Polycystic ovary syndrome in mitochondrial disorders due mtDNA or nDNA variants.

@nl

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Polycystic ovary syndrome in mitochondrial disorders due mtDNA or nDNA variants.

@en

Polycystic ovary syndrome in mitochondrial disorders due mtDNA or nDNA variants.

@nl

P1476

Polycystic ovary syndrome in mitochondrial disorders due mtDNA or nDNA variants.

@en

P2093

Josef Finsterer

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Sinda Zarrouk-Mahjoub

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P2860

Mutations in mitochondrial tRNA genes may be related to insulin resistance in women with polycystic ovary syndrome

Inherited mitochondrial disorders.

High prevalence of chronic thyroiditis in patients with polycystic ovary syndrome.

Polymorphisms in the TFAM and PGC1-α genes and their association with polycystic ovary syndrome among South Indian women.

Oocyte in-vitro maturation: BCL2 mRNA content in cumulus cells reflects oocyte competency.

The Mitochondrial tRNALeu(UUR) A3302G Mutation may be Associated With Insulin Resistance in Woman With Polycystic Ovary Syndrome.

Treatment strategies for women with polycystic ovary syndrome.

Point mutation in mitochondrial tRNA gene is associated with polycystic ovary syndrome and insulin resistance.

Analysis of mitochondrial DNA sequence variants in patients with polycystic ovary syndrome.

A 9-bp deletion homoplasmy in women with polycystic ovary syndrome revealed by mitochondrial genome-mutation screen.

P304

13-15

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P31

scholarly article

P407

English

P433

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P478

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P577

2018-01-15T00:00:00Z

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P698

29422990

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P921

polycystic ovary syndrome

P932

5801343

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