Evidence for Linkage of Human Primary Systemic Carnitine Deficiency with D5S436: A Novel Gene Locus on Chromosome 5q
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
Reference16 articles.
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2. Primary carnitine deficiency: heterozygote and intrafamilial phenotypic variation;Garavaglia;Neurology,1991
3. Multicenter trial of L-carnitine in maintenance hemodialysis patients. I. Carnitine concentrations and lipid effects;Golper;Kidney Int,1990
4. Infantile disease with microvesticular fatty infiltration of viscera spontaneously occurring in C3H-H2-2 strain of mouse with similarities to Reye's syndrome;Koizumi;Lab Anim,1988
5. Parametric and nonparametric linkage analysis: a unified multipoint approach;Kruglyak;Am J Hum Genet,1996
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