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Science 30 January 1998: Vol. 279. no. 5351, pp. 720 - 724 DOI: 10.1126/science.279.5351.720
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Reports
Alopecia Universalis Associated with a Mutation in the Human hairless Gene
Wasim Ahmad,
Muhammad Faiyaz ul Haque,
Valeria Brancolini,
Hui C. Tsou,
Sayed ul
Haque,
HaMut Lam,
Vincent M. Aita,
Jason Owen,
Michelle deBlaquiere,
Jorge Frank,
Peter B. Cserhalmi-Friedman,
Andrew Leask,
John A. McGrath,
Monica Peacocke,
Mahmud Ahmad,
Jurg Ott,
Angela M. Christiano
*
There are several forms of hereditary human hair loss, known
collectively as alopecias, the molecular bases of which are entirely unknown. A kindred with a rare, recessively inherited type of alopecia
universalis was used to search for a locus by homozygosity mapping, and
linkage was established in a 6-centimorgan interval on chromosome 8p12
(the logarithm of the odds favoring linkage score was 6.19). The human
homolog of a murine gene, hairless, was localized in this
interval by radiation hybrid mapping, and a missense mutation was found
in affected individuals. Human hairless encodes a putative
single zinc finger transcription factor protein with restricted
expression in the brain and skin.
W. Ahmad, H. C. Tsou, H. Lam, V. M. Aita, J. Frank,
P. B. Cserhalmi-Friedman, M. Peacocke, A. M. Christiano,
Department of Dermatology and Department of Genetics and Development,
Columbia University, 630 West 168 Street, VC-15-526, New York, NY
10032, USA.
M. F. ul Haque, S. ul Haque, M. Ahmad, Department of Biological
Sciences, Quaid-i-Azam University, Islamabad, Pakistan.
V. Brancolini and J. Ott, Laboratory for Statistical Genetics,
Rockefeller University, 1230 York Avenue, New York, NY 10021, USA.
J. Owen and M. deBlaquiere, Research Genetics, Inc., 2130 Memorial
Parkway SW, Huntsville, AL 35801, USA.
A. Leask, FibroGen, Inc., 260 Littlefield Avenue, South San Francisco,
CA 94080, USA.
J. A. McGrath, St. John's Institute of Dermatology, St. Thomas'
Hospital, Lambeth Palace Road, London, SE1 7EH, UK.
*
To whom correspondence should be addressed. E-mail:
amc65{at}columbia.edu
Read the Full Text
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