ATP7A
MIM.300011
Xq12-q13 HGNC:869 Entrez:538
Pathology
germline mutations of
ATP7A
in
Menkes disease
(
MIM.309400
)
occipital horn syndrome (
MIM.304150
)
X-linked congenital cutis laxa (
MIM.304150
)
See also
ATP7s
ATP7A
ATP7B
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germline mutations of ATP7A in germline mutations of ATP7A in