ロード中...
Molecular analyses of a tyrosinase-negative albino family.
Sequence analysis of the tyrosinase coding region from an individual with tyrosinase-negative oculocutaneous albinism revealed that the patient was a compound heterozygote. One allele carried a C--> A single-base substitution in codon 355 of exon 3, and the other carried a two-nucleotide deletion...
保存先:
| 主要な著者: | , , , , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
1993
|
| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1682201/ https://ncbi.nlm.nih.gov/pubmed/8430701 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|