Mutations in LPAR6/P2RY5 and LIPH are associated with woolly hair and/or hypotrichosis

Journal of the European Academy of Dermatology and Venereology

Volumn 27, Issue 5, 2013, Pages 545-549

  Kurban, M ^a   Wajid, M ^a   Shimomura, Y ^a   Christiano, A M ^a  

^a Och Spine at New York Presbyterian Hospitals   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE WOOLLY HAIR; CLINICAL FEATURE; CONTROLLED STUDY; GENE; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; HAIR DISEASE; HAPLOTYPE; HUMAN; HYPOTRICHOSIS; LIPH GENE; LPAR6 GENE; P2RY5 GENE; PAKISTAN; PRIORITY JOURNAL;

FEMALE; HAIR DISEASES; HAPLOTYPES; HUMANS; HYPOTRICHOSIS; LIPASE; MALE; MUTATION; PEDIGREE; RECEPTORS, LYSOPHOSPHATIDIC ACID; RECEPTORS, PURINERGIC P2;

EID: 84876153548     PISSN: 09269959     EISSN: 14683083     Source Type: Journal    
DOI: 10.1111/j.1468-3083.2012.04472.x     Document Type: Article

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