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

doi:10.1126/science.279.5351.720

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

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	720-724
Number of pages	5
Journal	Science
Volume	279
Issue number	5351
DOIs	https://doi.org/10.1126/science.279.5351.720
State	Published - Jan 30 1998
Externally published	Yes

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Ahmad, W., Ul Haque, M. F., Brancolini, V., Tsou, H. C., Ul Haque, S., Lam, H., Aita, V. M., Owen, J., DeBlaquiere, M., Frank, J., Cserhalmi-Friedman, P. B., Leask, A., McGrath, J. A., Peacocke, M., Ahmad, M., Ott, J., & Christiano, A. M. (1998). Alopecia universalis associated with a mutation in the human hairless gene. Science, 279(5351), 720-724. https://doi.org/10.1126/science.279.5351.720

Ahmad, W, Ul Haque, MF, Brancolini, V, Tsou, HC, Ul Haque, S, Lam, H, Aita, VM, Owen, J, DeBlaquiere, M, Frank, J, Cserhalmi-Friedman, PB, Leask, A, McGrath, JA, Peacocke, M, Ahmad, M, Ott, J & Christiano, AM 1998, 'Alopecia universalis associated with a mutation in the human hairless gene', Science, vol. 279, no. 5351, pp. 720-724. https://doi.org/10.1126/science.279.5351.720

@article{8b2982167e484ccba425985b84c5ac5d,

title = "Alopecia universalis associated with a mutation in the human hairless gene",

author = "Wasim Ahmad and \{Ul Haque\}, \{Muhammad Faiyaz\} and Valeria Brancolini and Tsou, \{Hui C.\} and \{Ul Haque\}, Sayed and Hamut Lam and Aita, \{Vincent M.\} and Jason Owen and Michelle DeBlaquiere and Jorge Frank and Cserhalmi-Friedman, \{Peter B.\} and Andrew Leask and McGrath, \{John A.\} and Monica Peacocke and Mahmud Ahmad and Jurg Ott and Christiano, \{Angela M.\}",

note = "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).",

year = "1998",

month = jan,

day = "30",

doi = "10.1126/science.279.5351.720",

language = "English",

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pages = "720--724",

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TY - JOUR

T1 - Alopecia universalis associated with a mutation in the human hairless gene

AU - Ahmad, Wasim

AU - Ul Haque, Muhammad Faiyaz

AU - Brancolini, Valeria

AU - Tsou, Hui C.

AU - Ul Haque, Sayed

AU - Lam, Hamut

AU - Aita, Vincent M.

AU - Owen, Jason

AU - DeBlaquiere, Michelle

AU - Frank, Jorge

AU - Cserhalmi-Friedman, Peter B.

AU - Leask, Andrew

AU - McGrath, John A.

AU - Peacocke, Monica

AU - Ahmad, Mahmud

AU - Ott, Jurg

AU - Christiano, Angela M.

N1 - 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).

PY - 1998/1/30

Y1 - 1998/1/30

UR - https://www.scopus.com/pages/publications/6844265562

UR - https://www.scopus.com/pages/publications/6844265562#tab=citedBy

U2 - 10.1126/science.279.5351.720

DO - 10.1126/science.279.5351.720

M3 - Article

SN - 0036-8075

VL - 279

SP - 720

EP - 724

JO - Science

JF - Science

IS - 5351

ER -

Alopecia universalis associated with a mutation in the human hairless gene

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