Title: | Compound heterozygous CACNA1H mutations associated with severe congenital amyotrophy. |
Journal : | Channels (Austin, Tex.), 13, n1 |
Authors: | Carter MT, Author ; McMillan HJ ; Tomin A ; Weiss N |
Material Type: | Article |
Publisher: | United States, 12/2019 |
Size: | p 153 |
Languages: | English |
Pubmed / DOI : | Pubmed : 31070086 / DOI : 10.1080/19336950.2019.1614415 |
N° Profil MNM : | 2019051 |
Link for e-copy: | http://www.ncbi.nlm.nih.gov/pubmed/31070086 |