Magliyah, M. S., Geuer, S., Alsalamah, A. K., Lenzner, S., Drasdo, M., & Schatz, P. (2021). Association of the Recurrent Rare Variant c.415T>C p.Phe139Leu in CLN5 With a Recessively Inherited Macular Dystrophy. JAMA Ophthalmol.
Παραπομπή Chicago StyleMagliyah, Moustafa S., Sinje Geuer, Abrar K. Alsalamah, Steffen Lenzner, Mojgan Drasdo, και Patrik Schatz. "Association of the Recurrent Rare Variant C.415T>C P.Phe139Leu in CLN5 With a Recessively Inherited Macular Dystrophy." JAMA Ophthalmol 2021.
Παραπομπή MLAMagliyah, Moustafa S., et al. "Association of the Recurrent Rare Variant C.415T>C P.Phe139Leu in CLN5 With a Recessively Inherited Macular Dystrophy." JAMA Ophthalmol 2021.
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