Homozygosity mapping of a gene responsible for gelatinous drop-like corneal dystrophy to chromosome 1p.

Gelatinous drop-like corneal dystrophy (GDLD) is a rare autosomal recessive disorder characterized clinically by grayish corneal deposits of amyloid and by severely impaired visual acuity. Most patients require corneal transplantation. To localize a gene responsible for GDLD, we performed linkage an...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Tsujikawa, M, Kurahashi, H, Tanaka, T, Okada, M, Yamamoto, S, Maeda, N, Watanabe, H, Inoue, Y, Kiridoshi, A, Matsumoto, K, Ohashi, Y, Kinoshita, S, Shimomura, Y, Nakamura, Y, Tano, Y
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1998
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377503/
https://ncbi.nlm.nih.gov/pubmed/9758629
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