Author/Creator: Kakakhel, Mashal - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Kakakhel, Mashal

1. Prph2 disease mutations lead to structural and functional defects in the RPE. Issue 5 (28th March 2022)

Authors:: Tebbe, Lars; Sakthivel, Haarthi; Makia, Mustafa S.; Kakakhel, Mashal; Conley, Shannon M.; Al‐Ubaidi, Muayyad R.; Naash, Muna I.
Journal:: FASEB journal
Issue:: Volume 36:Issue 5(2022)
Page Start:: n/a
Record Type:: Journal Article
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2. ROM1 contributes to phenotypic heterogeneity in PRPH2-associated retinal disease. (27th July 2020)

Authors:: Strayve, Daniel; Makia, Mustafa S; Kakakhel, Mashal; Sakthivel, Haarthi; Conley, Shannon M; Al-Ubaidi, Muayyad R; Naash, Muna I
Journal:: Human molecular genetics
Issue:: Volume 29:Number 16(2020)
Page Start:: 2708
Record Type:: Journal Article
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