bibliographic entry 6395140 [be/6395140]
https://w3id.org/oc/corpus/be/6395140

is a

• bibliographic reference

content

• Boycott, K.M, Beaulieu, C.L, Kernohan, K.D, Gebril, O.H, Mhanni, A, Chudley, A.E, Redl, D, Qin, W, Hampson, S, Kury, S. Autosomal-recessive intellectual disability with cerebellar atrophy syndrome caused by mutation of the manganese and zinc transporter gene SLC39A8, Am. J. Hum. Genet, 2015, 97, 886, 893, DOI: 10.1016/j.ajhg.2015.11.002, PMID: 26637978

references

• https://w3id.org/oc/corpus/br/1235552