PRJNA1128538 - Novel Bi-Allelic Variants in RINT1 Presenting As Early-Onset Pure Hereditary Spastic Paraplegia - OmicsDI

Genomics

Dataset Information

Novel Bi-Allelic Variants in RINT1 Presenting As Early-Onset Pure Hereditary Spastic Paraplegia

ABSTRACT: Novel Bi-Allelic Variants in RINT1 Presenting As Early-Onset Pure Hereditary Spastic Paraplegia

PROVIDER: PRJNA1128538 | ENA |

REPOSITORIES: ENA