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Article title matches
- Category:Leber, V (39 bytes)
1: List of pages with the keyword Leber, V - Category:Leber V (38 bytes)
1: List of pages with the keyword Leber V
Page text matches
- 1gzu (3,939 bytes)
11: ...N NMNA1_HUMAN] Defects in NMNAT1 are the cause of Leber congenital amaurosis 9 (LCA9) [MIM:[https://omim.... - 1jcn (4,031 bytes)
11: ...384941</ref> Defects in IMPDH1 are the cause of Leber congenital amaurosis type 11 (LCA11) [MIM:[https:... - 1kku (3,608 bytes)
10: ...N NMNA1_HUMAN] Defects in NMNAT1 are the cause of Leber congenital amaurosis 9 (LCA9) [MIM:[https://omim.... - 1kqn (3,849 bytes)
11: ...N NMNA1_HUMAN] Defects in NMNAT1 are the cause of Leber congenital amaurosis 9 (LCA9) [MIM:[https://omim.... - 1kqo (3,814 bytes)
11: ...N NMNA1_HUMAN] Defects in NMNAT1 are the cause of Leber congenital amaurosis 9 (LCA9) [MIM:[https://omim.... - 1kr2 (3,871 bytes)
11: ...N NMNA1_HUMAN] Defects in NMNAT1 are the cause of Leber congenital amaurosis 9 (LCA9) [MIM:[https://omim.... - 1s1n (4,792 bytes)
10: ...00]; also known as juvenile nephronophthisis with Leber amaurosis. SLSN is a renal-retinal disorder chara... - 2fim (4,771 bytes)
11: ...7620573</ref> Defects in TULP1 are the cause of Leber congenital amaurosis type 15 (LCA15) [MIM:[https:... - 9b8u (2,626 bytes)
11: ...ps://www.uniprot.org/uniprot/CRX_HUMAN CRX_HUMAN] Leber congenital amaurosis;Retinitis pigmentosa;Cone ro... - Sandbox Reserved 895 (30,318 bytes)
77: ...inent towards the retinoid cycle. Disease such as Leber congenital amaurosis (LCA) or retinal dystrophy d... - 3c5n (4,851 bytes)
11: ...7620573</ref> Defects in TULP1 are the cause of Leber congenital amaurosis type 15 (LCA15) [MIM:[https:... - 3d0e (9,789 bytes)
28: ...l inhibitor of AKT kinase.,Heerding DA, Rhodes N, Leber JD, Clark TJ, Keenan RM, Lafrance LV, Li M, Safon... - 3e87 (8,954 bytes)
28: ...t inhibitors of AKT kinase.,Rouse MB, Seefeld MA, Leber JD, McNulty KC, Sun L, Miller WH, Zhang S, Mintho... - 3e88 (12,809 bytes)
31: ...t inhibitors of AKT kinase.,Rouse MB, Seefeld MA, Leber JD, McNulty KC, Sun L, Miller WH, Zhang S, Mintho... - 3e8c (6,028 bytes)
26: ...t inhibitors of AKT kinase.,Rouse MB, Seefeld MA, Leber JD, McNulty KC, Sun L, Miller WH, Zhang S, Mintho... - 3e8d (9,012 bytes)
28: ...t inhibitors of AKT kinase.,Rouse MB, Seefeld MA, Leber JD, McNulty KC, Sun L, Miller WH, Zhang S, Mintho... - 3e8e (6,038 bytes)
26: ...t inhibitors of AKT kinase.,Rouse MB, Seefeld MA, Leber JD, McNulty KC, Sun L, Miller WH, Zhang S, Mintho... - 9i7u (3,836 bytes)
11: ...obinuria;Isolated cytochrome C oxidase deficiency;Leber hereditary optic neuropathy;MELAS. The disease is... - 3swy (2,723 bytes)
10: ...n this entry. Defects in CNGA3 may be a cause of Leber congenital amaurosis (LCA), a severe dystrophy of... - 8ev8 (4,641 bytes)
11: ...n this entry. Defects in CNGA3 may be a cause of Leber congenital amaurosis (LCA), a severe dystrophy of...
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