Identification of Mutations in the COL4A5 Collagen Gene in Alport Syndrome-Reference-Cited by-同舟云学术

Identification of Mutations in the COL4A5 Collagen Gene in Alport Syndrome

Published:1990-06-08 Issue:4960 Volume:248 Page:1224-1227
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

Barker David F.¹,Hostikka Sirkka Liisa²,Zhou Jing²,Chow Louise T.³,Oliphant Arnold R.¹,Gerken Steven C.¹,Gregory Martin C.⁴,Skolnick Mark H.¹,Atkin Curtis L.⁵,Tryggvason Karl²

Affiliation:

1. Department of Medical Informatics, University of Utah School of Medicine, Salt Lake City, UT 84132.

2. Biocenter and Department of Biochemistry, University of Oulu, SF-90570 Oulu, Finland.

3. Department of Biochemistry, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642.

4. Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City, UT 84132.

5. Department of Biochemistry, University of Utah School of Medicine, Salt Lake City, UT 84132.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference26 articles.

1. ATKIN, C.L., MAPPING OF ALPORT SYNDROME TO THE LONG ARM OF THE X-CHROMOSOME, AMERICAN JOURNAL OF HUMAN GENETICS 42: 249 (1988).

2. ATKIN, C.L., DIS KIDNEY: 617 (1988).

3. BARKER, D, A LOCUS ON CHROMOSOME 11P WITH MULTIPLE RESTRICTION SITE POLYMORPHISMS, AMERICAN JOURNAL OF HUMAN GENETICS 36: 1159 (1984).

4. BARKER D.F. unpublished data.

5. BOYD, C.D., THE SINGLE COPY GENE CODING FOR HUMAN ALPHA-1(IV) PROCOLLAGEN IS LOCATED AT THE TERMINAL END OF THE LONG ARM OF CHROMOSOME-13, HUMAN GENETICS 74: 121 (1986).

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