Ichthyosis Prematurity Syndrome Caused by a Novel Fatty Acid Transport Protein 4 Gene Mutation in a German Infant-Reference-Cited by-同舟云学术

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Ichthyosis Prematurity Syndrome Caused by a Novel Fatty Acid Transport Protein 4 Gene Mutation in a German Infant

Published:2011-06-01 Issue:6 Volume:147 Page:750
ISSN:0003-987X
Container-title:Archives of Dermatology
language:en
Short-container-title:Arch Dermatol

Author:

Inhoff Oliver,Hausser Ingrid,Schneider Stefan W.,Khnykin Denis,Jahnsen Frode L.,Sartoris Johann,Goerdt Sergij,Peitsch Wiebke K.

Publisher

American Medical Association (AMA)

Subject

Dermatology,General Medicine

Cited by 21 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis;Dermatology and Therapy;2024-08-07

2. Disorders of fatty acid homeostasis;Journal of Inherited Metabolic Disease;2024-05

3. Inherited Disorders of Cornification;Rook's Textbook of Dermatology;2024-03-19

4. Myeloid-specific fatty acid transport protein 4 deficiency induces a sex-dimorphic susceptibility for nonalcoholic steatohepatitis in mice fed a high-fat, high-cholesterol diet;American Journal of Physiology-Gastrointestinal and Liver Physiology;2023-05-01

5. Role of fatty acid transport protein 4 in metabolic tissues: insights into obesity and fatty liver disease;Bioscience Reports;2022-06-01

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