p.Leu636Pro mutation is associated with cystic fibrosis transmembrane conductance regulator-related disorders (congenital bilateral absence of vas deferens).
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p.Leu636Pro mutation is associated with cystic fibrosis transmembrane conductance regulator-related disorders (congenital bilateral absence of vas deferens).
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name
p.Leu636Pro mutation is associ ...... eral absence of vas deferens).
@en
p.Leu636Pro mutation is associ ...... ce regulator-related disorders
@nl
type
label
p.Leu636Pro mutation is associ ...... eral absence of vas deferens).
@en
p.Leu636Pro mutation is associ ...... ce regulator-related disorders
@nl
prefLabel
p.Leu636Pro mutation is associ ...... eral absence of vas deferens).
@en
p.Leu636Pro mutation is associ ...... ce regulator-related disorders
@nl
P2093
P2860
P356
P1476
p.Leu636Pro mutation is associ ...... eral absence of vas deferens).
@en
P2093
Carmela Colangelo
Domenico Dell'Edera
Donatello Salvatore
Giuseppina Smaldore
P2860
P304
P356
10.1111/IJU.12801
P577
2015-05-05T00:00:00Z