Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups-Reference-Cited by-同舟云学术

Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups

Published:1995-07 Issue:1 Volume:127 Page:13-22
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Moser Ann B.,Rasmussen Magnhild,Naidu Sakkubai,Watkins Paul A.,McGuinness Martina,Hajra Amiya K.,Chen Grace,Raymond Gerald,Liu Angela,Gordon Donald,Garnaas Karen,Walton David S.,Skjeldal Ola H.,Guggenheim Mary Anne,Jackson Laird G.,Elias Ellen Roy,Moser Hugo W.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference58 articles.

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3. A novel, cleavable peroxisomal targeting signal at the amino-terminus of the rat 3-ketoacyl-CoA thiolase;Swinkels;EMBO J,1991

4. Peroxisomal membrane ghosts in Zellweger syndrome: aberrant organelle assembly;Santos;Science,1988

5. Genetic complementation in heterokaryons of human fibroblasts defective in cobalamin metabolism;Gravel;Proc Natl Acad Sci USA,1975

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