Identification of a recurrent nonsense mutation in HR gene responsible for atrichia with papular lesions in two Kashmiri families
Ali, Ghazanfar, Awan, Naheed Bashir, Sadia, Khawaja, Abdul Waheed, Foo, Jia Nee, Khor, Chiea Chuen, Chang, Chu‐Hua, Chew, Elaine GuoYan, Kiani, Farhat Rafique, Jelani, Musharraf
Published in The journal of gene medicine (01.05.2020)
Published in The journal of gene medicine (01.05.2020)
Get full text
Journal Article
Identification of a Novel Homozygous Missense (c.443A>T:p.N148I) Mutation in BBS2 in a Kashmiri Family with Bardet-Biedl Syndrome
Ali, Ghazanfar, Sadia, Foo, Jia Nee, Nasir, Abdul, Chang, Chu-Hua, Chew, Elaine GuoYan, Latif, Zahid, Azeem, Zahid, Ain-ul-Batool, Syeda, Kazmi, Syed Akif Raza, Awan, Naheed Bashir, Khan, Abdul Hameed, Rehman, Fazal-Ur, Khalid, Madiha, Wali, Abdul, Sarwar, Samina, Akhtar, Wasim, Ahmed Abbasi, Ansar, Nisar, Rameez
Published in BioMed research international (2021)
Published in BioMed research international (2021)
Get full text
Journal Article
A Recurrent Nonsense Mutation in NECTIN4 Underlying Ectodermal Dysplasia-Syndactyly Syndrome with a Novel Phenotype in a Consanguineous Kashmiri Family
Ali, Ghazanfar, Sadia, Sadia, Ain-ul- Batool, Syeda, Azeem, Zahid, Awan, Naheed Bashir, Kazmi, Syed Akif Raza, Ur- Rehman, Zia, Anjum, Zeeshan, Ur- Rehman, Fazal, Wali, Abdul, Khan, Kafaitullah, Zaman, Nasib, Ayub, Muhammad, Sajid, Muhammad, Hassan, Noor
Published in Genetics Research (2023)
Published in Genetics Research (2023)
Get full text
Journal Article
Digital Platforms for Open Innovation: An Outlook from Technology Firms
Get full text
Conference Proceeding
Transferring Knowledge for Product Innovation: Analysis of Firm's Capabilities
Get full text
Conference Proceeding