Author： Sandoval N. Bauer D. Brenner V. Coy J.F. Drescher B. Kioschis P. Korn B. Nyakatura G. Poustka A. Reichwald K. Rosenthal A. Platzer M.
Publisher： Academic Press
ISSN： 0888-7543
Source： Genomics, Vol.35, Iss.2, 1996-07, pp. : 383-385
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Abstract
During the course of a large-scale sequencing project in Xq28, a human creatine transporter (CRTR) gene was discovered. The gene is located approximately 36 kb centromeric to ALD. The gene contains 13 exons and spans about 8.5 kb of genomic DNA. Since the creatine transporter has a prominent function in muscular physiology, it is a candidate gene for Barth syndrome and infantile cardiomyopathy mapped to Xq28.
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