Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Saisuda Noojaroen"'
Autor:
Lukana Ngiwsara, Duangrurdee Wattanasirichaigoon, Thipwimol Tim-Aroon, Kitiwan Rojnueangnit, Saisuda Noojaroen, Arthaporn Khongkraparn, Phannee Sawangareetrakul, James R. Ketudat-Cairns, Ratana Charoenwattanasatien, Voraratt Champattanachai, Chulaluck Kuptanon, Suthipong Pangkanon, Jisnuson Svasti
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-11 (2019)
Abstract Background Pompe disease is a lysosomal storage disorder caused by the deficiency of acid alpha-glucosidase (EC. 3.2.1.20) due to mutations in human GAA gene. The objective of the present study was to examine clinical and molecular character
Externí odkaz:
https://doaj.org/article/20abc3ca858c4e58874ef006f623ebd5
Autor:
Duangrurdee Wattanasirichaigoon, Kitiwan Rojnueangnit, Suthipong Pangkanon, Thipwimol Tim-Aroon, Saisuda Noojaroen, Ratana Charoenwattanasatien, Voraratt Champattanachai, Jisnuson Svasti, Lukana Ngiwsara, Phannee Sawangareetrakul, James R. Ketudat-Cairns, Arthaporn Khongkraparn, Chulaluck Kuptanon
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-11 (2019)
BMC Medical Genetics
BMC Medical Genetics
BackgroundPompe disease is a lysosomal storage disorder caused by the deficiency of acid alpha-glucosidase (EC. 3.2.1.20) due to mutations in humanGAAgene. The objective of the present study was to examine clinical and molecular characteristics of in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7025b4896632a2cd016cfa1158bf5c67
http://link.springer.com/article/10.1186/s12881-019-0878-8
http://link.springer.com/article/10.1186/s12881-019-0878-8