Frameshift Sequence Variants in the Human Lipase-H Gene Causing Hypotrichosis-Reference-Cited by-同舟云学术

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Frameshift Sequence Variants in the Human Lipase-H Gene Causing Hypotrichosis

Published:2015-12-08 Issue:1 Volume:33 Page:e40-e42
ISSN:0736-8046
Container-title:Pediatric Dermatology
language:en
Short-container-title:Pediatr Dermatol

Author:

Mehmood Sabba¹,Shah Sayed Hajan²,Jan Abid¹,Younus Muhammad¹,Ahmad Farooq¹,Ayub Muhammad³,Ahmad Wasim¹

Affiliation:

1. Department of Biochemistry; Faculty of Biological Sciences; Quaid-i-Azam University Islamabad; Islamabad Pakistan

2. Center for Human Genetics and Molecular Medicine; Sindh Institute of Urology and Transplantation; Karachi Pakistan

3. Institute of Biochemistry; University of Baluchistan; Quetta Pakistan

Funder

Pakistan Academy of Sciences

Higher Education Commission, Pakistan

Publisher

Wiley

Subject

Dermatology,Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/pde.12727/fullpdf

Reference5 articles.

1. A novel locus for autosomal recessive form of hypotrichosis maps to chromosome 3q26.33-q27.3;Aslam;J Med Genet,2004

2. G protein coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth;Pasternack;Nat Genet,2008

3. Mutations in the lipase-H gene causing autosomal recessive hypotrichosis and woolly hair;Mehmood;Australas J Dermatol,2015

4. Founder mutations in the lipase H gene in families with autosomal recessive woolly hair/hypotrichosis;Shimomura;J Invest Dermatol,2009

5. Novel mutations in G protein coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3);Azeem;Hum Genet,2008

Cited by 4 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. Isolated autosomal recessive woolly hair/hypotrichosis: genetics, pathogenesis and therapies;Journal of the European Academy of Dermatology and Venereology;2021-06-04

2. Novel small‐insertion mutation in the LIPH gene in a patient with autosomal recessive woolly hair/hypotrichosis;The Journal of Dermatology;2020-09-09

3. Druggable Lysophospholipid Signaling Pathways;Druggable Lipid Signaling Pathways;2020

4. Novel sequence variants in the LIPH and LPAR6 genes underlies autosomal recessive woolly hair/hypotrichosis in consanguineous families;Congenital Anomalies;2017-06-12

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