| Title |
|
|
|
Phenotypes in siblings with homozygous mutations of TRAPPC9 and/or MCPH1 support a bifunctional model of MCPH1
| |
| Author |
|
|
|
| |
| Abstract |
|
|
| | |
| Language |
|
|
|
English
| |
| Source (journal) |
|
|
|
Molecular genetics & genomic medicine | |
| Publication |
|
|
|
2018
| |
| ISSN |
|
|
|
2324-9269
| |
| Volume/pages |
|
|
|
6:4(2018), p. 660-665
| |
| ISI |
|
|
|
000441004000019
| |
| Pubmed ID |
|
|
|
29693325
| |
| Full text (Publisher's DOI) |
|
|
| | |
| Full text (open access) |
|
|
| | |
|