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Familial AD accounts for 5%10% of AD patients, where inherited autosomal dominant mutations in three genes have been considered as the primary causes of familial AD: these include mutations in the genes encoding -amyloid precursor protein (APP) and presenilins (PS1 and PS2

Biol Open 8(2):bio037655 [DOI] [PMC free article] [PubMed] [Google Scholar] Coca-Pelaz A, Shah JP, Hernandez-Prera JC, Ghossein RA, Rodrigo JP, Hartl DM, Olsen KD, Shaha AR, Zafereo M, Suarez C (2020) Papillary thyroid canceraggressive variants and impact on management: a narrative review

PMID: 40756949 (view on PubMed) Stable Gastric Pentadecapeptide BPC 157 as a Therapy for the Disabled Myotendinous Junctions in Rats

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