Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits-Reference-Cited by-同舟云学术

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Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits

Published:2010-09-16 Issue:11 Volume:31 Page:E1851-E1860
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Horn Denise,Kapeller Johannes,Rivera-Brugués Núria,Moog Ute,Lorenz-Depiereux Bettina,Eck Sebastian,Hempel Maja,Wagenstaller Janine,Gawthrope Alex,Monaco Anthony P.,Bonin Michael,Riess Olaf,Wohlleber Eva,Illig Thomas,Bezzina Connie R.,Franke Andre,Spranger Stephanie,Villavicencio-Lorini Pablo,Seifert Wenke,Rosenfeld Jochen,Klopocki Eva,Rappold Gudrun A.,Strom Tim M.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Cited by 127 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. FOXP1 regulates the development of excitatory synaptic inputs onto striatal neurons and induces phenotypic reversal with reinstatement;Science Advances;2024-05-03

2. Auditory discrimination learning and acoustic cue weighing in female zebra finches with localized FoxP1 knockdowns;Journal of Neurophysiology;2024-05-01

3. FOXP1 regulates the development of excitatory synaptic inputs onto striatal neurons and induces phenotypic reversal with reinstatement;2023-10-24

4. The challenges in the interpretation of genetic variants detected by genomics techniques in patients with congenital anomalies;Journal of Clinical Laboratory Analysis;2023-09

5. The enteric nervous system deficits in autism spectrum disorder;Frontiers in Neuroscience;2023-08-24

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