Unravelling the genetic basis of retinal dystrophies in Pakistani consanguineous families

Abstract Background Retinitis Pigmentosa (RP) is a clinically and genetically progressive retinal dystrophy associated with severe visual impairments and sometimes blindness, the most common syndromic form of which is Usher syndrome (USH). This study aimed to further increase understanding of the sp...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής

Κύριοι συγγραφείς:	Muhammad Marwan, Muhammad Dawood, Mukhtar Ullah, Irfan Ullah Shah, Niamat Khan, Muhammad Taimur Hassan, Muhammad Karam, Lettie E. Rawlins, Emma L Baple, Andrew H. Crosby, Shamim Saleha
Μορφή:	Artigo
Γλώσσα:	Inglês
Έκδοση:	BMC 2023-05-01
Σειρά:	BMC Ophthalmology
Θέματα:	Retinitis pigmentosa Usher syndrome Pakistani PED6C MYO7A RHO
Διαθέσιμο Online:	https://doi.org/10.1186/s12886-023-02948-8
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