Publications:

Inherited Disorders of Thyroid Hormone Metabolism Defect Caused by the Dysregulation of Selenoprotein Expression.

Frontiers In Endocrinology

Lee, Kyu Won KW; Shin, Yoochan Y; Lee, Sungahn S; Lee, Sihoon S

Publication Date: 2021

Variant appearance in text: SECISBP2: 2037G>T; E679D

PubMed Link: 35126314

Variant Present in the following documents:

• Main text
• fendo-12-803024.pdf

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Human Genetic Disorders Resulting in Systemic Selenoprotein Deficiency.

International Journal Of Molecular Sciences

Schoenmakers, Erik E; Chatterjee, Krishna K

Publication Date: 2021-11-29

Variant appearance in text: SECISBP2: E679D

PubMed Link: 34884733

Variant Present in the following documents:

• Main text
• ijms-22-12927.pdf

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Human Genetic Disorders Resulting in Systemic Selenoprotein Deficiency.

International Journal Of Molecular Sciences

Schoenmakers, Erik E; Chatterjee, Krishna K

Publication Date: 2021-11-29

Variant appearance in text: SECISBP2: E679D

PubMed Link: 34884733

Variant Present in the following documents:

• Main text
• ijms-22-12927.pdf

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Human Disorders Affecting the Selenocysteine Incorporation Pathway Cause Systemic Selenoprotein Deficiency.

Antioxidants & Redox Signaling

Schoenmakers, Erik E; Chatterjee, Krishna K

Publication Date: 2020-09-01

Variant appearance in text: SECISBP2: E679D

PubMed Link: 32295391

Variant Present in the following documents:

• Main text

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Clinical and Molecular Analysis in 2 Families With Novel Compound Heterozygous SBP2 (SECISBP2) Mutations.

The Journal Of Clinical Endocrinology And Metabolism

Fu, Jiao J; Korwutthikulrangsri, Manassawee M; Gönç, E Nazli EN; Sillers, Laura L; Liao, Xiao-Hui XH; Alikaşifoğlu, Ayfer A; Kandemir, Nurgün N; Menucci, Maria Belen MB; Burman, Kenneth D KD; Weiss, Roy E RE; Dumitrescu, Alexandra M AM

Publication Date: 2020-03-01

Variant appearance in text: SBP2: 2037G>T

PubMed Link: 32084277

Variant Present in the following documents:

• Main text

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