Novel mutations in the P2RY5 gene in one Turkish and two Indian patients presenting with hypotrichosis and woolly hair

Archives of Dermatological Research

Volumn 301, Issue 8, 2009, Pages 621-624

  Pasternack, Sandra M ^a   Murugusundram, Sundaram ^b   Eigelshoven, Sibylle ^c   Müller, Melanie ^a   Kruse, Roland ^c   Lehmann, Percy ^d   Betz, Regina C ^a  

^a UNIVERSITY OF BONN   (Germany)

^b Skin Hair and Nail Clinic   (India)

^c HEINRICH HEINE UNIVERSITY   (Germany)

^d UNIVERSITY OF WITTEN HERDECKE   (Germany)

Author keywords

Hair loss; Hypotrichosis simplex; Mutation analysis; P2RY5 gene

Indexed keywords

G PROTEIN COUPLED RECEPTOR; LIPASE H; PROTEIN; TRIACYLGLYCEROL LIPASE; UNCLASSIFIED DRUG;

ALOPECIA; AMINO ACID SUBSTITUTION; ARTICLE; CASE REPORT; CHILD; CLINICAL FEATURE; DISEASE COURSE; DNA EXTRACTION; ELECTRON MICROSCOPY; ETHNICITY; FAMILY; FEMALE; FRAMESHIFT MUTATION; GENE DELETION; GENE DUPLICATION; GENE MUTATION; HAIR DISEASE; HAIR GROWTH; HAIR TEXTURE; HUMAN; HYPOTRICHOSIS; INDIAN; MICROSCOPY; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; RISK FACTOR; SCHOOL CHILD; TURKEY (REPUBLIC); WOOLLY HAIR;

BASE SEQUENCE; CHILD; FEMALE; HAIR; HUMANS; HYPOTRICHOSIS; INDIA; LIPASE; MOLECULAR SEQUENCE DATA; MUTATION; RECEPTORS, PURINERGIC P2; TURKEY;

EID: 69049105281     PISSN: 03403696     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00403-009-0971-5     Document Type: Article

References (12)

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