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vitelliform macular dystrophy/proline

Povezava se shrani v odložišče
ČlankiKliničnih preskušanjPatenti
2 rezultatov
We have cloned and characterized a novel gene (C11orf9) mapping to chromosome 11q12-->q13.1. The transcript was initially identified as a partial cDNA sequence in the course of constructing a transcript map of the region between markers D11S1765 and uteroglobin known to encompass the gene causing

Cloning and characterization of the murine Vmd2 RFP-TM gene family.

Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
Mutations in the human vitelliform macular dystrophy type 2 (VMD2) gene are known to cause autosomal dominant Best macular dystrophy (BMD), a degenerative disorder of the central retina. VMD2, together with VMD2L1, VMD2L2 and VMD2L3, belong to a closely related gene family characterized by several
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