Mutations in the hair cortex keratin hhb6 cause the inherited hair disease monilethrix

Nature Genetics

Volumn 16, Issue 4, 1997, Pages 372-374

  Winter, H ^a   Rogers, M A ^a   Langbein, L ^a   Stevens, H P ^a   Leigh, I M ^a   Labraze, C ^a   Roul, S ^a   Taieb, A ^a   Krieg, T ^a   Schweizer, J ^a  

^a GERMAN CANCER RESEARCH CENTER DKFZ   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

KERATIN;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CLINICAL ARTICLE; DNA SEQUENCE; FAMILIAL DISEASE; FEMALE; GENE MUTATION; HAIR DISEASE; HETEROZYGOSITY; HUMAN; MALE; PEDIGREE; POINT MUTATION; PRIORITY JOURNAL;

ADOLESCENT; CHILD; FEMALE; GLUTAMIC ACID; HAIR DISEASES; HETEROZYGOTE; HUMANS; KERATINS; LYSINE; MALE; MIDDLE AGED; MUTATION; PEDIGREE;

EID: 0030747138     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng0897-372     Document Type: Article

References (25)