Expanding the phenotypic spectrum of TRIT1 mutatins, a cause of severe autosomal recessive microcephaly
| Affiliation auteurs | !!!! Error affiliation !!!! |
| Titre | Expanding the phenotypic spectrum of TRIT1 mutatins, a cause of severe autosomal recessive microcephaly |
| Type de publication | Journal Article |
| Year of Publication | 2019 |
| Auteurs | Smol T., Brunelle P., Boute-Benejean O., Basseti J.A, Figeac M., Faivre L., Petit F., Thauvin-Robinet C., Thomas Q., Tran-Mau-Them F., Manouvrier-Hanu S., Ghoumid J. |
| Journal | EUROPEAN JOURNAL OF HUMAN GENETICS |
| Volume | 27 |
| Pagination | 1407-1408 |
| Date Published | OCT |
| Type of Article | Meeting Abstract |
| ISSN | 1018-4813 |