Frequency of the cholesteryl ester storage disease commonLIPAE8SJM mutation (c.894G>A) in various racial and ethnic groups-Reference-Cited by-同舟云学术

Frequency of the cholesteryl ester storage disease commonLIPAE8SJM mutation (c.894G>A) in various racial and ethnic groups

Published:2013-07-29 Issue:3 Volume:58 Page:958-965
ISSN:0270-9139
Container-title:Hepatology
language:en
Short-container-title:Hepatology

Author:

Scott Stuart A.¹,Liu Benny,Nazarenko Irina¹,Martis Suparna¹,Kozlitina Julia²,Yang Yao¹,Ramirez Charina³,Kasai Yumi¹,Hyatt Tommy⁴,Peter Inga¹,Desnick Robert J.¹

Affiliation:

1. Department of Genetics and Genomic Sciences; Icahn School of Medicine at Mount Sinai; New York; NY

2. McDermott Center for Human Growth and Development; University of Texas Southwestern Medical Center; Dallas; TX

3. Department of Pediatrics; University of Texas Southwestern Medical Center; Dallas; TX

4. Howard Hughes Medical Institute; University of Texas Southwestern Medical Center; Dallas; TX

Publisher

Wiley

Subject

Hepatology

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2. Wolman disease and its treatment;Wolman;Clin Pediatr (Phila),1995

3. Genetic and biochemical evidence that CESD and Wolman disease are distinguished by residual lysosomal acid lipase activity;Aslanidis;Genomics,1996

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