A novel mutation in LPAR6 causes autosomal recessive hypotrichosis of the scalp

Clinical and Experimental Dermatology

Volumn 36, Issue 2, 2011, Pages 188-194

  Nahum, S ^a   Morice Picard, F ^b   Taieb, A ^b   Sprecher, E ^a,c,d  

^a TECHNION ISRAEL INSTITUTE OF TECHNOLOGY   (Israel)

^b INSERM   (France)

^c TEL AVIV SOURASKY MEDICAL CENTER   (Israel)

^d TEL AVIV UNIVERSITY   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

LYSOPHOSPHATIDYLCHOLINE;

ADOLESCENT; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CASE REPORT; GENE; GENE MAPPING; GENE MUTATION; HOMOZYGOSITY; HUMAN; HYPOTRICHOSIS; LPAR6 GENE; MALE; MICROSATELLITE MARKER; MISSENSE MUTATION; POINT MUTATION; PRIORITY JOURNAL; SCALP;

ADOLESCENT; AMINO ACID SUBSTITUTION; DNA MUTATIONAL ANALYSIS; FEMALE; GENOTYPE; HUMANS; HYPOTRICHOSIS; MALE; MICROSATELLITE REPEATS; MUTATION, MISSENSE; PEDIGREE; RECEPTORS, LYSOPHOSPHATIDIC ACID; SCALP;

EID: 79951633111     PISSN: 03076938     EISSN: 13652230     Source Type: Journal    
DOI: 10.1111/j.1365-2230.2010.03944.x     Document Type: Article

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