Molecular genetic analysis of two families with keratosis follicularis spinulosa decalvans: refinement of gene localization and evidence for genetic heterogeneity-Reference-Cited by-同舟云学术

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Molecular genetic analysis of two families with keratosis follicularis spinulosa decalvans: refinement of gene localization and evidence for genetic heterogeneity

Published:1997-09-15 Issue:5-6 Volume:100 Page:520-524
ISSN:0340-6717
Container-title:Human Genetics
language:
Short-container-title:Human Genetics

Author:

Oosterwijk J. C.,Richard Gabriela,van der Wielen Michiel J. R.,van de Vosse E.,Harth Wolfgang,Sandkuijl Lodewijk A.,Bakker Egbert,van Ommen Gert-Jan B.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s004390050546.pdf

Cited by 24 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. Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V;Frontiers in Genetics;2021-07-12

2. ATP7A-Regulated Enzyme Metalation and Trafficking in the Menkes Disease Puzzle;Biomedicines;2021-04-06

3. The Role of Trichoscopy in Keratosis Follicularis Spinulosa Decalvans: Case Report and Review of the Literature;Skin Appendage Disorders;2020-10-12

4. Keratosis Pilaris and Darier Disease;Harper's Textbook of Pediatric Dermatology;2019-11-20

5. Genetic Abnormalities of the Cornea;Ophthalmic Genetic Diseases;2019

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