Literature DB >> 20015179

A novel deletion mutation in P2RY5/LPA(6) gene cause autosomal recessive woolly hair with hypotrichosis.

L Horev, B Saad-Edin, A Ingber, A Zlotogorski.   

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Year:  2009        PMID： 20015179     DOI： 10.1111/j.1468-3083.2009.03514.x

Source DB:  PubMed          Journal:  J Eur Acad Dermatol Venereol        ISSN： 0926-9959            Impact factor:   6.166


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  3 in total

1.  To the Root of the Curl: A Signature of a Recent Selective Sweep Identifies a Mutation That Defines the Cornish Rex Cat Breed.

Authors:  Barbara Gandolfi; Hasan Alhaddad; Verena K Affolter; Jeffrey Brockman; Jens Haggstrom; Shannon E K Joslin; Amanda L Koehne; James C Mullikin; Catherine A Outerbridge; Wesley C Warren; Leslie A Lyons
Journal:  PLoS One       Date:  2013-06-27       Impact factor: 3.240

2.  In silico analysis of missense mutations in LPAR6 reveals abnormal phospholipid signaling pathway leading to hypotrichosis.

Authors:  Syed Irfan Raza; Dost Muhammad; Abid Jan; Raja Hussain Ali; Mubashir Hassan; Wasim Ahmad; Sajid Rashid
Journal:  PLoS One       Date:  2014-08-13       Impact factor: 3.240

3.  A novel mutation in the Lipase H gene underlies autosomal recessive hypotrichosis and woolly hair.

Authors:  Muhammad Tariq; Aysha Azhar; Shahid Mahmood Baig; Niklas Dahl; Joakim Klar
Journal:  Sci Rep       Date:  2012-10-12       Impact factor: 4.379
  3 in total

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