MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update

By  

HUMAN MUTATION, Vol. 39, Iss. 3, 2018-03 ,pp. : 333-344

John Wiley & Sons Inc

Access to resources Recommend Favorite

Development of a Magnetic Electrochemical Bar Code Array for Point Mutation Detection in the H5N1 Neuraminidase Gene

By Krejcova Ludmila   Hynek David   Kopel Pavel   Merlos Rodrigo Miguel Angel   Adam Vojtech   Hubalek Jaromir   Babula Petr   Trnkova Libuse   Kizek Rene  

Viruses, Vol. 5, Iss. 7, 2013-07 ,pp. : 1719-1739

MDPI

Access to resources Recommend Favorite

De Novo Mutation in the SCN5A Gene Associated with Brugada Syndrome

By  

Cellular Physiology and Biochemistry, Vol. 36, Iss. 6, 2015-07 ,pp. : 2250-2262

Karger

Access to resources Recommend Favorite

McArdle Disease: Update of Reported Mutations and Polymorphisms in the PYGM Gene

By  

HUMAN MUTATION, Vol. 36, Iss. 7, 2015-07 ,pp. : 669-678

John Wiley & Sons Inc

Access to resources Recommend Favorite

Mutation of the Emx-1 Homeobox Gene Disrupts the Corpus Callosum

By Qiu M.   Anderson S.   Chen S.   Meneses J.J.   Hevner R.   Kuwana E.   Pedersen R.A.   Rubenstein J.L.R.  

Developmental Biology, Vol. 178, Iss. 1, 1996-08 ,pp. : 174-178

Academic Press

Access to resources Recommend Favorite