A Novel Loss-of-Function Mutation in HOXB1 Associated with...

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Molecular Syndromology 2017 / 6

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

Vahidi Mehrjardi, Mohammad Yahya, Maroofian, Reza, Kalantar, Seyed M., Jaafarinia, Mojtaba, Chilton, John, Dehghani, Mohammadreza
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Language:
english
Journal:
Molecular Syndromology
DOI:
10.1159/000477752
Date:
June, 2017
File:
PDF, 231 KB
english, 2017
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