Exclusion of the C/D box snoRNA gene cluster HBII-52 from a major role in Prader–Willi syndrome

SNORD115

Síndrome de Prader-Willi

متلازمة برادر- فيلي

Microdeletion syndrome

Microdeletion syndrome is a syndrome caused by a chromosomal deletion (< 5Mb) spanning several genes that is too small to be detected by conventional cytogenetic methods…

Ube3a-ATS

The human UBE3A-ATS is expressed as a part of LNCAT mainly from the paternal allele in the central nervous system (CNS).

Prader-Willi-Syndrom

Small nucleolar RNA SNORD115

SNORD115 (also known as HBII-52) is a non-coding RNA (ncRNA) molecule known as a small nucleoloar RNA which usually functions in guiding the modification of other non-codi…