Mesh : Humans Male Adrenoleukodystrophy / genetics diagnosis Heterozygote Karyotype ATP Binding Cassette Transporter, Subfamily D, Member 1

来  源:   DOI:10.1001/jamaneurol.2024.0061

Abstract:
This case report studies a 12-year-old boy with a family history of X-linked adrenal leukodystrophy and his 8-year-old younger brother.
摘要:
该病例报告研究了一名具有X连锁肾上腺脑白质营养不良家族史的12岁男孩及其8岁弟弟。
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