Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Abdul Wahab, Siti Aishah"'
Autor:
Abdul Wahab, Siti Aishah, Yakob, Yusnita, Mohd Khalid, Mohd Khairul Nizam, Ali, Noraishah, Leong, Huey Yin, Ngu, Lock Hock, RAMACHANDRAN, VASUDEVAN
Publikováno v:
Genetics Research; 9/13/2022, p1-7, 7p
Autor:
Abdul Wahab, Siti Aishah1, Yakob, Yusnita1, Abdul Azize, Nor Azimah1, Md Yunus, Zabedah2, Huey Yin, Leong3, Mohd Khalid, Mohd Khairul Nizam1, Lock Hock, Ngu3
Publikováno v:
BioMed Research International. 9/8/2016, Vol. 2016, p1-5. 5p.
Autor:
Hiew Fu Liong1 hiewfl@gmail.com, Abdul Wahab, Siti Aishah2, Yusnita Yakob2, Ngu Lock Hock3, Wong Kum Thong4, Viswanathan, Shanthi1
Publikováno v:
Case Reports in Neurological Medicine. 2014, p1-6. 6p.
Autor:
Fu Liong, Hiew, Abdul Wahab, Siti Aishah, Yakob, Yusnita, Lock Hock, Ngu, Thong, Wong Kum, Viswanathan, Shanthi
Publikováno v:
Case Reports in Neurological Medicine.
Pompe’s disease (acid maltase deficiency, glycogen storage disease type II) is an autosomal recessive disorder caused by a deficiency of lysosomal acid α-1,4-glucosidase, resulting in excessive accumulation of glycogen in the lysosomes and cytopla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=hindawi_publ::2902953d63f382b6c7e8ac89ce664efe