Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Maha S. Al-Shammari"'
Autor:
Maha S. Al-Shammari, Rhaya Al-Ali, Nader Al-Balawi, Mansour S. Al-Enazi, Ali A. Al-Muraikhi, Fadi N. Busaleh, Ali S. Al-Sahwan, Abdulmohsen Al-Elq, Awatif N. Al-Nafaie, Jesu Francis Borgio, Sayed AbdulAzeez, Amein Al-Ali, Sadananda Acharya
Publikováno v:
Genetics and Molecular Biology, Vol 40, Iss 3, Pp 586-590 (2017)
Abstract Genome-wide association studies have identified several loci associated with an increased risk for cardiovascular disease (CVD) and type 2 diabetes (T2D). Polymorphisms within the KCNQ1 (potassium voltage-gated channel, KQT-like subfamily, m
Externí odkaz:
https://doaj.org/article/73a9fe912f344490a06bbed236ec3249
Autor:
Nicholas W. Wood, Saif Alshahrani, Dilek Colak, Michael C. Kruer, Kshitij Mankad, Zuhair Rahbeeni, Rozeena Huma, Khushnooda Ramzan, Rawan Almass, Stanislav Groppa, Moeenaldeen Al-Sayed, Indran Davagnanam, Fuad Almutairi, Maha S Al-Shammari, Maria Puiu, E Ghayoor Karimiani, N. Kaya, Stephanie Efthymiou, Nourelhoda A Haridy, M Beiraghi Toosi, Alya Qari, Muddathir H. Hamad, Mustafa A. Salih, Maysoon Alsagob, Somayeh Bakhtiari, Jessika Johannsen, Tatjana Bierhals, Reza Maroofian, Katja Kloth, Adela Chirita-Emandi, Henry Houlden, N T Malintan, Faiqa Imtiaz, Ibrahim A. Alorainy, Jana Vandrovcova, Laila AlQuait, Hamad Al-Zaidan, Viorica Chelban
Publikováno v:
European Journal of Neurology
Background and purpose\ud Hypomyelinating leukodystrophies are a heterogeneous group of genetic disorders with a wide spectrum of phenotypes and a high rate of genetically unsolved cases. Bi‐allelic mutations in NKX6‐2 were recently linked to spa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a074b70a1bf1d6a7a437cc5a7084b5ca
https://openaccess.sgul.ac.uk/id/eprint/111215/6/Chelban_et_al-2019-European_Journal_of_Neurology.pdf
https://openaccess.sgul.ac.uk/id/eprint/111215/6/Chelban_et_al-2019-European_Journal_of_Neurology.pdf
Autor:
Awatif N. Al-Nafaie, Sayed AbdulAzeez, Ali S Al-Sahwan, Sadananda Acharya, Abdulmohsen H. Al-Elq, Maha S Al-Shammari, Amein K. Al-Ali, Fadi N Busaleh, Rhaya Al-Ali, Mansour S Al-Enazi, Nader Al-Balawi, Jesu Francis Borgio, Ali A Al-Muraikhi
Publikováno v:
Genetics and Molecular Biology v.40 n.3 2017
Genetics and Molecular Biology
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology, Volume: 40, Issue: 3, Pages: 586-590, Published: 31 AUG 2017
Genetics and Molecular Biology, Vol 40, Iss 3, Pp 586-590 (2017)
Genetics and Molecular Biology
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology, Volume: 40, Issue: 3, Pages: 586-590, Published: 31 AUG 2017
Genetics and Molecular Biology, Vol 40, Iss 3, Pp 586-590 (2017)
Genome-wide association studies have identified several loci associated with an increased risk for cardiovascular disease (CVD) and type 2 diabetes (T2D). Polymorphisms within the KCNQ1 (potassium voltage-gated channel, KQT-like subfamily, member 1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af5357454cde3a4fbf2f7aaa94b70b87
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572017000400586
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572017000400586