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...

詳細記述

保存先:
書誌詳細
主要な著者: Park, K C, Chintamaneni, C D, Halaban, R, Witkop, C J, Kwon, B S
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!