Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Abdul Rashid Silawati"'
Autor:
Teguh Haryo Sasongko, Abdul Qawee Mahyoob Rani, Salmi Abdul Razak, Wee Teik Keng, Abdul Rashid Silawati, Nor Azni Yahya, Nur Farrah Dila Ismail, Siti Nabilahuda Mohd Azlan, Lock Hock Ngu, Z A M H Zabidi-Hussin, Narazah Mohd Yusoff, Chia Boon Hock, Nik Mohd Ariff Nik Abdul Malik
Publikováno v:
The Journal of molecular diagnostics : JMD. 19(2)
Tuberous sclerosis complex (TSC) is an autosomal dominant neurocutaneous disorder characterized by tumor growth in multiple organs and caused by mutations in either TSC1 or TSC2 genes. Because of their relatively large genomic sizes, absence of hotsp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82a405bc6f6ff28feb89de368a960e99
https://pubmed.ncbi.nlm.nih.gov/28087349
https://pubmed.ncbi.nlm.nih.gov/28087349
Autor:
Jafar Mohseni, Fatemeh Hayati, Teguh Haryo Sasongko, Abdul Razak Salmi, Lock Hock Ngu, Mohd Yusof Narazah, Nur Farrah Dila Ismail, Wee Teik Keng, Abdul Rashid Silawati, Abdulqawee Mahyoob Rani, Z A M H Zabidi-Hussin, Nik Mohd Ariff Nik Abdul Malik
Publikováno v:
Japanese journal of clinical oncology. 44(5)
Tuberous sclerosis complex is an autosomal dominant neurocutaneous disorder affecting multiple organs. Tuberous sclerosis complex is caused by mutation in either one of the two disease-causing genes, TSC1 or TSC2, encoding for hamartin and tuberin, r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f61f18f6c6f91b394d0fee5a439f81d
https://pubmed.ncbi.nlm.nih.gov/24683199
https://pubmed.ncbi.nlm.nih.gov/24683199