Mutation profiles of phenylketonuria in Quebec populations: evidence of stratification and novel mutations.
about
Sequence variation at the phenylalanine hydroxylase gene in the British Isles.Population genetics of hyperphenylalaninaemia resulting from phenylalanine hydroxylase deficiency in Portugal.Predominance of the T14484C mutation in French-Canadian families with Leber hereditary optic neuropathy is due to a founder effect.
P2860
Mutation profiles of phenylketonuria in Quebec populations: evidence of stratification and novel mutations.
description
1994 nî lūn-bûn
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1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
Mutation profiles of phenylket ...... ification and novel mutations.
@ast
Mutation profiles of phenylket ...... ification and novel mutations.
@en
type
label
Mutation profiles of phenylket ...... ification and novel mutations.
@ast
Mutation profiles of phenylket ...... ification and novel mutations.
@en
prefLabel
Mutation profiles of phenylket ...... ification and novel mutations.
@ast
Mutation profiles of phenylket ...... ification and novel mutations.
@en
P2093
P2860
P1476
Mutation profiles of phenylket ...... tification and novel mutations
@en
P2093
Laframboise R
Mascisch A
Scriver CR
P2860
P304
P407
P577
1994-08-01T00:00:00Z