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Exon splice enhancer mutation (GH-E32A) causes autosomal dominant growth hormone deficiency. [electronic resource] by
- Petkovic, Vibor
- Lochmatter, Didier
- Turton, James
- Clayton, Peter E
- Trainer, Peter J
- Dattani, Mehul T
- Eblé, Andrée
- Robinson, Iain C
- Flück, Christa E
- Mullis, Primus E
Producer: 20080102
In:
The Journal of clinical endocrinology and metabolism vol. 92
Availability: No items available.
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11900.
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