(Q21261476)
Statements
Exome sequencing identifies a novel mutation in PIK3R1 as the cause of SHORT syndrome (English)
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Carlos López-Otín
Carlos
López-Otín
1 reference
1 reference
Annachiara De Sandre-Giovannoli
Annachiara
De Sandre-Giovannoli
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1 reference
1 reference
Diana A Puente
1 reference
Joaquín Fernández-Toral
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Sabine Sigaudy
1 reference
Anwar Baban
1 reference
Gloria Velasco
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2014
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15
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1
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51
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1 reference