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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
2011-7-22
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pubmed:abstractText |
Autosomal recessive hypotrichosis/woolly hair is a rare genetic hair loss disorder characterized by sparse scalp hair/woolly hair, sparse to absent eyebrows and eyelashes, sparse axillary and body hair in affected individuals. This form of hair loss results from mutations in either LPAR6 or LIPH gene.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1365-2230
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pubmed:author |
pubmed-author:AhmadWW,
pubmed-author:AliGG,
pubmed-author:AliNN,
pubmed-author:AnsaiTT,
pubmed-author:AyubMM,
pubmed-author:BasitSS,
pubmed-author:HabibRR,
pubmed-author:Kamran-Ul-Hassan NaqviSS,
pubmed-author:KhanSS,
pubmed-author:MiiSS,
pubmed-author:ODDOO,
pubmed-author:ShafiqueSS,
pubmed-author:Umm-e-Kalsoom,
pubmed-author:WallLL,
pubmed-author:WasikCC,
pubmed-author:YaminTT
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pubmed:copyrightInfo |
© The Author(s). CED © 2011 British Association of Dermatologists.
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pubmed:issnType |
Electronic
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pubmed:volume |
36
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
652-4
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pubmed:meshHeading |
pubmed-meshheading:21426374-Adult,
pubmed-meshheading:21426374-Child,
pubmed-meshheading:21426374-Consanguinity,
pubmed-meshheading:21426374-DNA Mutational Analysis,
pubmed-meshheading:21426374-Exons,
pubmed-meshheading:21426374-Female,
pubmed-meshheading:21426374-Genes, Recessive,
pubmed-meshheading:21426374-Genetic Linkage,
pubmed-meshheading:21426374-Genetic Predisposition to Disease,
pubmed-meshheading:21426374-Genotype,
pubmed-meshheading:21426374-Hair Diseases,
pubmed-meshheading:21426374-Humans,
pubmed-meshheading:21426374-Hypotrichosis,
pubmed-meshheading:21426374-Lipase,
pubmed-meshheading:21426374-Male,
pubmed-meshheading:21426374-Mutation,
pubmed-meshheading:21426374-Pakistan,
pubmed-meshheading:21426374-Pedigree,
pubmed-meshheading:21426374-Phenotype,
pubmed-meshheading:21426374-Receptors, Lysophosphatidic Acid
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pubmed:year |
2011
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pubmed:articleTitle |
Mutations in the LPAR6 and LIPH genes underlie autosomal recessive hypotrichosis/woolly hair in 17 consanguineous families from Pakistan.
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pubmed:affiliation |
Department of Biochemistry, Faculty of Biological Sciences, Quaid-i-Azam University Islamabad, Pakistan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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