首页> 外文OA文献 >Thirty-eight-year follow-up of two sibling Lipoid Congenital Adrenal Hyperplasia patients due to homozygous Steroidogenic Acute Regulatory (STARD1) protein Mutation. Molecular structure and modeling of the STARD1 L275P mutation.

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Thirty-eight-year follow-up of two sibling Lipoid Congenital Adrenal Hyperplasia patients due to homozygous Steroidogenic Acute Regulatory (STARD1) protein Mutation. Molecular structure and modeling of the STARD1 L275P mutation.

机译：由于纯合子类固醇激素调节（sTaRD1）蛋白突变，对两个同胞类脂质先天性肾上腺增生患者进行了38年的随访。 sTaRD1 L275p突变的分子结构和模型。

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Jean-Guy Lehoux;
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年度 2016
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1. Thirty-Eight-Year Follow-Up of Two Sibling Lipoid Congenital Adrenal Hyperplasia Patients Due to Homozygous Steroidogenic Acute Regulatory (STARD1) Protein Mutation. Molecular Structure and Modeling of the STARD1 L275P Mutation [J] . Khalil Khoury, Elie Barbar, Youssef Ainmelk, Frontiers in Neuroscience . 2016,第2012期

机译：由于纯合类固醇激素急性调节（STARD1）蛋白突变，两名兄弟姐妹类脂质先天性肾上腺增生患者的三十八年随访。 STARD1 L275P突变的分子结构和建模
2. Homozygous Q258X Mutation in the Steroidogenic Acute Regulatory Gene in a Japanese Patient with Congenital Lipoid Adrenal Hyperplasia [J] . ATSUKO NAGASHIMA-MIYOKAWA, AYAKO TANAE, ITSURO HIBI, Endocrine journal . 1997,第3期

机译：纯合子Q258X突变的日本先天性类脂性肾上腺皮质增生患者中的类固醇急性调节基因。
3. A Novel Mutation of the Steroidogenic Acute Regulatory Protein (StAR) Gene in a Japanese Patient with Congenital Lipoid Adrenal Hyperplasia [J] . Katsura Ishizu, Junko Tsubaki, Wakako Jyo, Clinical Pediatric Endocrinology . 2008,第1期

机译：日本先天性类脂质肾上腺皮质增生患者中类固醇急性调节蛋白（StAR）基因的新型突变。
4. Thirty-Eight-Year Follow-Up of Two Sibling Lipoid Congenital Adrenal Hyperplasia Patients Due to Homozygous Steroidogenic Acute Regulatory (STARD1) Protein Mutation. Molecular Structure and Modeling of the STARD1 L275P Mutation [O] . Khalil Khoury, Elie Barbar, Youssef Ainmelk, 2016

机译：由于同型类固醇激素急性调节（STARD1）蛋白突变导致的两个兄弟姐妹类脂性先天性肾上腺增生患者的三十八年随访。 STARD1 L275P突变的分子结构和建模
5. Thirty-Eight-Year Follow-Up of Two Sibling Lipoid Congenital Adrenal Hyperplasia Patients Due to Homozygous Steroidogenic Acute Regulatory (STARD1) Protein Mutation. Molecular Structure and Modeling of the STARD1 L275P Mutation [O] . Khalil Khoury, Elie Barbar, Youssef Ainmelk, 2016

机译：由于纯合子类固醇激素急性调节（sTaRD1）蛋白质突变导致的两个兄弟姐妹先天性肾上腺增生患者的38年随访。 sTaRD1 L275p突变的分子结构和模型

Thirty-eight-year follow-up of two sibling Lipoid Congenital Adrenal Hyperplasia patients due to homozygous Steroidogenic Acute Regulatory (STARD1) protein Mutation. Molecular structure and modeling of the STARD1 L275P mutation.

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