In Silico Analysis of Missense Mutations in LPAR6 Reveals Abnormal Phospholipid Signaling Pathway Leading to Hypotrichosis

Autosomal recessive hypotrichosis is a rare genetic irreversible hair loss disorder characterized by sparse scalp hair, sparse to absent eyebrows and eyelashes, and sparse axillary and body hair. The study, presented here, established genetic linkage in four families showing similar phenotypes to ly...

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Detalles Bibliográficos
Autores principales: Raza, Syed Irfan, Muhammad, Dost, Jan, Abid, Ali, Raja Hussain, Hassan, Mubashir, Ahmad, Wasim, Rashid, Sajid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4132050/
https://www.ncbi.nlm.nih.gov/pubmed/25119526
http://dx.doi.org/10.1371/journal.pone.0104756

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4132050/
https://www.ncbi.nlm.nih.gov/pubmed/25119526
http://dx.doi.org/10.1371/journal.pone.0104756

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