Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Jakob Kuriakose"'
Autor:
Gonzalo Perez-Siles, Anthony Cutrupi, Melina Ellis, Jakob Kuriakose, Sharon La Fontaine, Di Mao, Motonari Uesugi, Reinaldo I. Takata, Carlos E. Speck-Martins, Garth Nicholson, Marina L. Kennerson, Annemieke Aartsma-Rus, James Dowling, Maaike van Putten
Publikováno v:
Disease Models & Mechanisms, Vol 13, Iss 2 (2020)
ATP7A encodes a copper-transporting P-type ATPase and is one of 23 genes in which mutations produce distal hereditary motor neuropathy (dHMN), a group of diseases characterized by length-dependent axonal degeneration of motor neurons. We have generat
Externí odkaz:
https://doaj.org/article/96cf025b67e84cd9944cad361424728a
Publikováno v:
Advances in experimental medicine and biology. 1383
Many gastrointestinal motility disorders arise due to defects in the enteric nervous system. Achalasia and gastroparesis are two extremely debilitating digestive diseases of the upper gastrointestinal tract caused in part by damage or loss of the nit
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 9783031058424
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5bce9d088d25ad4ad9f432d0edbb8e41
https://doi.org/10.1007/978-3-031-05843-1_29
https://doi.org/10.1007/978-3-031-05843-1_29
Autor:
Gonzalo Perez-Siles, Anthony Cutrupi, Melina Ellis, Jakob Kuriakose, Sharon La Fontaine, Di Mao, Motonari Uesugi, Reinaldo I. Takata, Carlos E. Speck-Martins, Garth Nicholson, Marina L. Kennerson, Annemieke Aartsma-Rus, James Dowling, Maaike van Putten
Publikováno v:
Disease Models & Mechanisms
Disease Models & Mechanisms, Vol 13, Iss 2 (2020)
Disease Models & Mechanisms, Vol 13, Iss 2 (2020)
ATP7A encodes a copper-transporting P-type ATPase and is one of 23 genes in which mutations produce distal hereditary motor neuropathy (dHMN), a group of diseases characterized by length-dependent axonal degeneration of motor neurons. We have generat