TY  - JOUR
AU  - Ramos-Molina, Bruno
AU  - Molina-Vega, María
AU  - Fernández-García, José C
AU  - Creemers, John W
PY  - 2018
DO  - 10.3390/genes9060288
SN  - 2073-4425
UR  - https://hdl.handle.net/10668/26489
T2  - Genes
AB  - Prader⁻Willi syndrome (PWS) is a complex genetic disorder that, besides cognitive impairments, is characterized by hyperphagia, obesity, hypogonadism, and growth impairment. Proprotein convertase subtilisin/kexin type 1 (PCSK1) deficiency, a rare...
LA  - en
KW  - PCSK1 deficiency
KW  - Prader–Willi syndrome
KW  - hyperphagia
KW  - hypothalamus
KW  - obesity
TI  - Hyperphagia and Obesity in Prader⁻Willi Syndrome: PCSK1 Deficiency and Beyond?
TY  - research article
VL  - 9
ER  -