Barceló A, Girós M, Sarde C O, Pintos G, Mandel J L, Pàmpols T, Estivill X
Servei de Genètica, Hospital Clínic, Barcelona, Spain.
Hum Genet. 1995 Feb;95(2):235-7. doi: 10.1007/BF00209412.
Adrenoleukodystrophy (ALD) is an X-linked disease, characterised by an alteration of the peroxisomal beta-oxidation of the very long chain fatty acids. The ALD gene has been identified and mutations have been detected in ALD patients. We report here a new missense mutation in the ALD gene of a male patient, predicting a tyrosine to serine substitution at codon 174 (mutation Y174S). The mother of the ALD patient does not have the Y174S mutation in her leukocyte DNA, indicating that Y174S arose de novo in the patient. Y174S is the first reported de novo mutation in the ALD gene.
肾上腺脑白质营养不良(ALD)是一种X连锁疾病,其特征是极长链脂肪酸的过氧化物酶体β氧化发生改变。ALD基因已被鉴定,并且在ALD患者中检测到了突变。我们在此报告一名男性患者的ALD基因中出现了一种新的错义突变,预测在密码子174处酪氨酸被丝氨酸取代(Y174S突变)。该ALD患者的母亲白细胞DNA中没有Y174S突变,这表明Y174S是患者新发的突变。Y174S是首次报道的ALD基因新发突变。