A Novel Mutation in the CYP11B1 Gene Causes Steroid 11β-Hydroxylase Deficient Congenital Adrenal Hyperplasia with Reversible Cardiomyopathy.
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A Novel Mutation in the CYP11B1 Gene Causes Steroid 11β-Hydroxylase Deficient Congenital Adrenal Hyperplasia with Reversible Cardiomyopathy.
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name
A Novel Mutation in the CYP11B ...... ith Reversible Cardiomyopathy.
@ast
A Novel Mutation in the CYP11B ...... ith Reversible Cardiomyopathy.
@en
type
label
A Novel Mutation in the CYP11B ...... ith Reversible Cardiomyopathy.
@ast
A Novel Mutation in the CYP11B ...... ith Reversible Cardiomyopathy.
@en
prefLabel
A Novel Mutation in the CYP11B ...... ith Reversible Cardiomyopathy.
@ast
A Novel Mutation in the CYP11B ...... ith Reversible Cardiomyopathy.
@en
P2093
P2860
P356
P1476
A Novel Mutation in the CYP11B ...... ith Reversible Cardiomyopathy.
@en
P2093
Abdullah A Alhayani
Ali M Alsuheel
Ayed A Shati
Brain F Meyer
Hessa M Gilban
Minjing Zou
Mohammad A Alqahtani
Saleh M Al-Qahtani
P2860
P304
P356
10.1155/2015/595164
P577
2015-07-22T00:00:00Z