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Wilcken DEL, Wang XL, Sim AS, and McCredie RM (1996)

Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin

The WNK1 gene is located on chromosome 12p13.33 and is composed of 31 exons that generate four alternatively spliced mRNAs with the 2382 amino acid isoform 1 being the most common

For example, testosterone replacement therapy combined with BPC-157 for injury recovery and CJC-1295 for anti-aging