Strong founder effect for a transglutaminase 1 gene mutation in lamellar ichthyosis and congenital ichthyosiform erythroderma from Norway-Reference-Cited by-同舟云学术

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Strong founder effect for a transglutaminase 1 gene mutation in lamellar ichthyosis and congenital ichthyosiform erythroderma from Norway

Published:1998-11 Issue:6 Volume:6 Page:589-596
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Pigg Maritta,Jr Tobias Gedde-Dahl,Cox Diane,Haußer Ingrid,Anton-Lamprecht Ingrun,Dahl Niklas

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/5200224.pdf

Cited by 51 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. Autosomal recessiveALOX12Bgene and consecutive collodion baby;BMJ Case Reports;2024-03

2. Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs;Frontiers in Pharmacology;2023-11-09

3. High TGM1 Allelic Heterogeneity causing Lamellar ichthyosis in a small geographic area in South Mexico: Another Example of the “Réunion Paradox”;European Journal of Medical Genetics;2023-10

4. Ophthalmic findings in patients with autosomal recessive lamellar ichthyosis due to TGM1 mutations in an isolated population;International Ophthalmology;2023-08-05

5. Ophthalmic Findings in Patients with Autosomal Recessive Lamellar Ichthyosis due to TGM1 Mutations in an Isolated Population;2023-04-05

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