Molecular genetic investigations identify new clinical phenotypes associated with BCS1L-related mitochondrial disease / Oláhová, M; Ceccatelli Berti, C; Collier, Jj; Alston, Cl; Jameson, E; Jones, Sa; Edwards, N; He, L; Chinnery, Pf; Horvath, R; Goffrini, P; Taylor, Rw; Sayer, Ja.. - In: HUMAN MOLECULAR GENETICS ONLINE. - ISSN 1460-2083. - 28:22(2019), pp. 3766-3776. [10.1093/hmg/ddz202]

Molecular genetic investigations identify new clinical phenotypes associated with BCS1L-related mitochondrial disease

Ceccatelli Berti C;Goffrini P;
2019-01-01

2019
Molecular genetic investigations identify new clinical phenotypes associated with BCS1L-related mitochondrial disease / Oláhová, M; Ceccatelli Berti, C; Collier, Jj; Alston, Cl; Jameson, E; Jones, Sa; Edwards, N; He, L; Chinnery, Pf; Horvath, R; Goffrini, P; Taylor, Rw; Sayer, Ja.. - In: HUMAN MOLECULAR GENETICS ONLINE. - ISSN 1460-2083. - 28:22(2019), pp. 3766-3776. [10.1093/hmg/ddz202]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11381/2866965
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