PubMed (OMIM) for id: 411553

Year	Number of Results
1955	1
1956	1
1964	1
1965	1
1966	2
1968	1
1969	1
1977	3
1980	1
1986	1
1988	2
1990	1
1992	2
1994	4
1995	1
1996	1
1997	2
1998	3
1999	1
2000	3
2001	1
2002	1
2005	1
2023	0

1

Optical coherence tomography in Best's disease: an observational case report.

Vedantham V, Ramasamy K. Vedantham V, et al. Am J Ophthalmol. 2005 Feb;139(2):351-3. doi: 10.1016/j.ajo.2004.07.039. Am J Ophthalmol. 2005. PMID: 15734003

2

Hereditary degeneration of the macula; occurring in five generations.

DAVIS CT, HOLLENHORST RW. DAVIS CT, et al. Am J Ophthalmol. 1955 May;39(5):637-43. doi: 10.1016/0002-9394(55)90035-0. Am J Ophthalmol. 1955. PMID: 14361622 No abstract available.

3

HEREDITARY VITELLINE MACULAR DEGENERATION. A CLINICAL AND FUNCTIONAL EVALUATION OF A NEW PEDIGREE WITH VARIABLE EXPRESSIVITY AND DOMINANT INHERITANCE.

BRALEY AE, SPIVEY BE. BRALEY AE, et al. Arch Ophthalmol. 1964 Dec;72:743-62. doi: 10.1001/archopht.1964.00970020743003. Arch Ophthalmol. 1964. PMID: 14205432 No abstract available.

4

Macular cysts; a dominantly inherited affection with a progressive course.

SORSBY A, SAVORY M, DAVEY JB, FRASER RJ. SORSBY A, et al. Br J Ophthalmol. 1956 Mar;40(3):144-58. doi: 10.1136/bjo.40.3.144. Br J Ophthalmol. 1956. PMID: 13315939 Free PMC article. No abstract available.

5

The vitelliform macular dystrophy protein defines a new family of chloride channels.

Sun H, Tsunenari T, Yau KW, Nathans J. Sun H, et al. Proc Natl Acad Sci U S A. 2002 Mar 19;99(6):4008-13. doi: 10.1073/pnas.052692999. Proc Natl Acad Sci U S A. 2002. PMID: 11904445 Free PMC article.

6

Sequence variation and disease in the wake of the draft human genome.

Goodstadt L, Ponting CP. Goodstadt L, et al. Hum Mol Genet. 2001 Oct 1;10(20):2209-14. doi: 10.1093/hmg/10.20.2209. Hum Mol Genet. 2001. PMID: 11673403 Review.

7

Bestrophin, the product of the Best vitelliform macular dystrophy gene (VMD2), localizes to the basolateral plasma membrane of the retinal pigment epithelium.

Marmorstein AD, Marmorstein LY, Rayborn M, Wang X, Hollyfield JG, Petrukhin K. Marmorstein AD, et al. Proc Natl Acad Sci U S A. 2000 Nov 7;97(23):12758-63. doi: 10.1073/pnas.220402097. Proc Natl Acad Sci U S A. 2000. PMID: 11050159 Free PMC article.

8

Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration.

Krämer F, White K, Pauleikhoff D, Gehrig A, Passmore L, Rivera A, Rudolph G, Kellner U, Andrassi M, Lorenz B, Rohrschneider K, Blankenagel A, Jurklies B, Schilling H, Schütt F, Holz FG, Weber BH. Krämer F, et al. Eur J Hum Genet. 2000 Apr;8(4):286-92. doi: 10.1038/sj.ejhg.5200447. Eur J Hum Genet. 2000. PMID: 10854112

9

VMD2 mutations in vitelliform macular dystrophy (Best disease) and other maculopathies.

White K, Marquardt A, Weber BH. White K, et al. Hum Mutat. 2000;15(4):301-8. doi: 10.1002/(SICI)1098-1004(200004)15:4<301::AID-HUMU1>3.0.CO;2-N. Hum Mutat. 2000. PMID: 10737974 Review.

10

Evaluation of the Best disease gene in patients with age-related macular degeneration and other maculopathies.

Allikmets R, Seddon JM, Bernstein PS, Hutchinson A, Atkinson A, Sharma S, Gerrard B, Li W, Metzker ML, Wadelius C, Caskey CT, Dean M, Petrukhin K. Allikmets R, et al. Hum Genet. 1999 Jun;104(6):449-53. doi: 10.1007/s004390050986. Hum Genet. 1999. PMID: 10453731

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