Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Adrenal Insufficiency and ABCD1[original query] |
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Identification of novel SNPs of ABCD1, ABCD2, ABCD3, and ABCD4 genes in patients with X-linked adrenoleukodystrophy (ALD) based on comprehensive resequencing and association studies with ALD phenotypes. Neurogenetics 2011 Feb 12 (1): 41-50. Matsukawa Takashi, Asheuer Muriel, Takahashi Yuji, Goto Jun, Suzuki Yasuyuki, Shimozawa Nobuyuki, Takano Hiroki, Onodera Osamu, Nishizawa Masatoyo, Aubourg Patrick, Tsuji Sho |
X-linked adrenoleukodystrophy: phenotype-genotype correlation in hemizygous males and heterozygous females with ABCD1 mutations. Neuro endocrinology letters 2021 9 42 (5): 359-367. Zemanova Marketa, Chrastina Petr, Dvorakova Lenka, Reboun Martin, Vlaskova Hana, Jahnova Helena, El-Lababidi Nabil, Cepova Jana, Honzik Tomas, Zeman Ji |
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