Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome-Reference-Cited by-同舟云学术

Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome

Published:2016-12-12 Issue:1 Volume:127 Page:293-305
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:

Author:

Burnett Lisa C.,LeDuc Charles A.,Sulsona Carlos R.,Paull Daniel,Rausch Richard,Eddiry Sanaa,Carli Jayne F. Martin,Morabito Michael V.,Skowronski Alicja A.,Hubner Gabriela,Zimmer Matthew,Wang Liheng,Day Robert,Levy Brynn,Fennoy Ilene,Dubern Beatrice,Poitou Christine,Clement Karine,Butler Merlin G.,Rosenbaum Michael,Salles Jean Pierre,Tauber Maithe,Driscoll Daniel J.,Egli Dieter,Leibel Rudolph L.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference71 articles.

1. Birth prevalence of Prader-Willi syndrome in Australia

2. Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings

3. Prader-Willi syndrome

4. Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster

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