A Novel Loss-of-Function Mutation in HOXB1 Associated with Autosomal Recessive Hereditary Congenital Facial Palsy in a Large Iranian Family-Reference-Cited by-同舟云学术

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A Novel Loss-of-Function Mutation in HOXB1 Associated with Autosomal Recessive Hereditary Congenital Facial Palsy in a Large Iranian Family

Published:2017 Issue:5 Volume:8 Page:261-265
ISSN:1661-8769
Container-title:Molecular Syndromology
language:en
Short-container-title:Mol Syndromol

Author:

Vahidi Mehrjardi Mohammad Yahya,Maroofian Reza,Kalantar Seyed M.,Jaafarinia Mojtaba,Chilton John,Dehghani Mohammadreza

Publisher

S. Karger AG

Subject

Genetics (clinical),Genetics

Cited by 8 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. Facial Palsy;Smith's Recognizable Patterns of Human Deformation;2025

2. Two novel compound heterozygous HOXB1 variants in congenital facial palsy: A case report and a brief review of the literature;American Journal of Medical Genetics Part A;2024-09-05

3. Expanding the Phenotype of Hereditary Congenital Facial Paresis Type 3;International Journal of Molecular Sciences;2023-12-21

4. Abnormal outer hair cell efferent innervation in Hoxb1-dependent sensorineural hearing loss;PLOS Genetics;2023-09-22

5. Echoencephalography of Möbius sequence: A congenital cranial dysinnervation disorder with brainstem calcifications;Journal of Neuroimaging;2022-11-09

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