Literature DB >> 19852579

Mutations in KIF21A and PHOX2A are absent in 16 patients with congenital vertical incomitant strabismus.

Arif O Khan, Dania S Khalil, Latifa J Al-Sharif, Nada A Al-Tassan.   

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Year:  2009        PMID： 19852579     DOI： 10.3109/13816810903183613

Source DB:  PubMed          Journal:  Ophthalmic Genet        ISSN： 1381-6810            Impact factor:   1.803


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  4 in total

1.  Recessive mutations in COL25A1 are a cause of congenital cranial dysinnervation disorder.

Authors:  Jameela M A Shinwari; Arif Khan; Salma Awad; Zakia Shinwari; Ayodele Alaiya; Mohamad Alanazi; Asma Tahir; Coralie Poizat; Nada Al Tassan
Journal:  Am J Hum Genet       Date:  2014-12-11       Impact factor: 11.025

2.  MiR-326 regulates cell proliferation and migration in lung cancer by targeting phox2a and is regulated by HOTAIR.

Authors:  Rong Wang; Xiaofeng Chen; Tongpeng Xu; Rui Xia; Liang Han; Wenming Chen; Wei De; Yongqian Shu
Journal:  Am J Cancer Res       Date:  2016-01-15       Impact factor: 6.166

3.  Retinal Dysfunction in Patients with Congenital Fibrosis of the Extraocular Muscles Type 2.

Authors:  Arif O Khan; Mohammed Almutlaq; Darren T Oystreck; Elizabeth C Engle; Khaled Abu-Amero; Thomas Bosley
Journal:  Ophthalmic Genet       Date:  2014-06-18       Impact factor: 1.803

4.  Lack of KIF21A mutations in congenital fibrosis of the extraocular muscles type I patients from consanguineous Saudi Arabian families.

Authors:  Arif O Khan; Jameela Shinwari; Aisha Omar; Latifa Al-Sharif; Dania S Khalil; Mohammed Alanazi; Abdullah Al-Amri; Nada Al Tassan
Journal:  Mol Vis       Date:  2011-01-20       Impact factor: 2.367
  4 in total

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