Authors:
Siegel, Dawn H.
Ashton, Gabrielle H.S.
Penagos, Homero G.
Lee, James V.
Feiler, Heidi S.
Wilhelmsen, Kirk C.
South, Andrew P.
Smith, Frances J.D.
Prescott, Alan R.
Wessagowit, Vesarat
Oyama, Noritaka
Akiyama, Masashi
Al Aboud, Daifullah
Al Aboud, Khalid
Al Githami, Ahmad
Al Hawsawi, Khalid
Al Ismaily, Abla
Al-Suwaid, Raouf
Atherton, David J.
Caputo, Ruggero
Fine, Jo-David
Frieden, Ilona J.
Fuchs, Elaine
Haber, Richard M.
Harada, Takashi
Kitajima, Yasuo
Mallory, Susan B.
Ogawa, Hideoki
Sahin, Sedef
Shimizu, Hiroshi
Suga, Yasushi
Tadini, Gianluca
Tsuchiya, Kikuo
Wiebe, Colin B.
Wojnarowska, Fenella
Zaghloul, Adel B.
Hamada, Takahiro
Mallipeddi, Rajeev
Eady, Robin A.J.
Irwin McLean, W.H.
McGrath, John A.
Epstein, Ervin H. , Jr.
Citation: H. Siegel, Dawn et al., Loss of Kindlin-1, a Human Homolog of the Caenorhabditis elegans Actin.Extracellular-Matrix Linker Protein UNC-112, Causes Kindler Syndrome, American journal of human genetics , 73(1), 2003, pp. 174-187
Authors:
Der Perng, Ming
Su, Mu
Wen, Shu Fang
Li, Rong
Gibbon, Terry
Prescott, Alan R.
Brenner, Michael
Quinlan, Roy A.
Citation: Der Perng, Ming et al., The Alexander Disease.Causing Glial Fibrillary Acidic Protein Mutant, R416W, Accumulates into Rosenthal Fibers by a Pathway That Involves Filament Aggregation and the Association of .B-Crystallin and HSP27, American journal of human genetics , 79(2), 2006, pp. 197-213