4H Syndrome With Late-Onset Growth Hormone Deficiency Caused by POLR3A Mutations-Reference-Cited by-同舟云学术

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4H Syndrome With Late-Onset Growth Hormone Deficiency Caused by POLR3A Mutations

Published:2012-07-01 Issue:7 Volume:69 Page:
ISSN:0003-9942
Container-title:Archives of Neurology
language:en
Short-container-title:Arch Neurol

Author:

Potic Ana,Brais Bernard,Choquet Karine,Schiffmann Raphael,Bernard Geneviève

Publisher

American Medical Association (AMA)

Subject

Clinical Neurology,Arts and Humanities (miscellaneous)

Cited by 46 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Endocrine Care of a 19-year-old Woman With Isolated Hypogonadotropic Hypogonadism due to 4H Syndrome;AACE Clinical Case Reports;2024-08

3. Case report: neuropsychological assessment in a patient with 4H leukodystrophy;The Clinical Neuropsychologist;2023-11-16

4. Distinct Interaction Modes for the Eukaryotic RNA Polymerase Alpha-like Subunits;Molecular and Cellular Biology;2023-05-24

5. A homozygous POLR1A variant causes leukodystrophy and affects protein homeostasis;Brain;2023-03-14

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