New GAA mutations in japanese patients with GSDII (pompe disease)-Reference-Cited by-同舟云学术

New GAA mutations in japanese patients with GSDII (pompe disease)

Published:2003-10 Issue:4 Volume:29 Page:284-287
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Pipo Judy R,Feng Jian-Hua,Yamamoto Toshiyuki,Ohsaki Yuki,Nanba Eiji,Tsujino Seiichi,Sakuragawa Norio,Martiniuk Frank,Ninomiya Haruaki,Oka Akira,Ohno Kousaku

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health

Reference18 articles.

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4. Isolation of a cDNA human alpha-D-glucosidase and detection of genetic heterogeity for mRNA in three alpha glucosidase deficient patients;Martiniuk;Proc Natl Acad Sci USA,1986

5. Primary structure and processing of lysosomal alpha-glucosidase; homology with the intestinal sucrase-isomaltase complex;Hoefsloot;EMBO J,1988

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