Mutations in the LPAR6 and LIPH genes underlie autosomal recessive hypotrichosis/woolly hair in 17 consanguineous families from Pakistan

Clinical and Experimental Dermatology

Volumn 36, Issue 6, 2011, Pages 652-654

  Khan, S ^a   Habib, R ^a   Mir, H ^a   Umm E Kalsoom, ^a   Naz, G ^a   Ayub, M ^a   Shafique, S ^b   Yamin, T ^a   Ali, N ^a   Basit, S ^a   Wasif, N ^a   Kamran Ul Hassan Naqvi, S ^a   Ali, G ^a   Wali, A ^c   Ansar, M ^a   Ahmad, W ^a  

^a QUAID I AZAM UNIVERSITY   (Pakistan)

^b UNIVERSITY OF BALOCHISTAN   (Pakistan)

^c BALOCHISTAN UNIVERSITY OF INFORMATION TECHNOLOGY   (Pakistan)

Author keywords

[No Author keywords available]

Indexed keywords

LIPASE MEMBER H PROTEIN; LYSOPHOSPHATIDIC ACID RECEPTOR 6 PROTEIN; PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; DNA SEQUENCE; GENE AMPLIFICATION; GENE MUTATION; GENETIC LINKAGE; GENOTYPE; HAPLOTYPE; HUMAN; HYPOTRICHOSIS; MICROSATELLITE MARKER; MUTATIONAL ANALYSIS; PAKISTAN; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

ADULT; CHILD; CONSANGUINITY; DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; GENES, RECESSIVE; GENETIC LINKAGE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HAIR DISEASES; HUMANS; HYPOTRICHOSIS; LIPASE; MALE; MUTATION; PAKISTAN; PEDIGREE; PHENOTYPE; RECEPTORS, LYSOPHOSPHATIDIC ACID;

EID: 79960580136     PISSN: 03076938     EISSN: 13652230     Source Type: Journal    
DOI: 10.1111/j.1365-2230.2011.04014.x     Document Type: Article

References (8)

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