Add missing PMID

Author: bbimber

mGAP/resources/views/phenotypes.html

@@ -11,7 +11,7 @@
                 ['Nervous system','Vision','Achromotopsia','PDE6C','c.1694G>A; p.Arg565Gln','Moshiri et al., 2019:30667376'],
                 ['Nervous system','Vision','Age-related macular degeneration','HTRA1, ARMS2','','Francis  et al., 2008:18535016;Singh et al., 2009:19028492'],
                 ['Nervous system','Vision','Bardet-Beidl syndrome','BBS7','c.160delG; p.Ala54fs','Peterson et al., 2019:31589838'],
-                ['Nervous system','Vision','Oculocuateous albinism','TYRP1','c.1,028A>G; p.Asp343Gly<br>c.1,244T>C; p.Leu415Pro','Peterson et al., 2023:'],
+                ['Nervous system','Vision','Oculocuateous albinism','TYRP1','c.1,028A>G; p.Asp343Gly<br>c.1,244T>C; p.Leu415Pro','Peterson et al., 2023:37522525'],
                 ['Nervous system','Vision','Oculocuateous albinism','TYR1','c.768C>G; p.His256Gln',''],
                 ['Nervous system','Vision','Coats-like retinopathy','','','Liu et al., 2015:25656754'],
                 ['Nervous system','Neurological','Batten disease','CLN7','c.769delA; p.Ile257LeufsTer36','McBride et al., 2018:30048804'],